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Moderne Probleme der Humangenetik

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Ergebnisse der Inneren Medizin und Kinderheilkunde

Part of the book series: Ergebnisse der Inneren Medizin und Kinderheilkunde ((KINDERHEILK. NF,volume 12))

Zusammenfassung

Das Thema „moderne Probleme der Humangenetik“ ist weit gespannt. Es erfordert vom Referenten, daß er eine Auswahl dessen trifft, was er für besonders wesentlich hält. Für diese Auswahl gibt es zwar objektive Kriterien; trotzdem ist es nicht zu vermeiden, daß sich in ihr die subjektive Meinung des Referenten widerspiegelt, die durch seine persönliche Eigenart, seine eigene Arbeitsrichtung, aber auch durch Zufälligkeiten seiner Entwicklung und Literaturkenntnis bestimmt ist.

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Literatur

  • Aird, I., H. H. Bentall and J. A. Fraser-Roberts: Relation between cancer of stomach and the ABO blood groups. Brit. med. J. 1953 I, 799–801.

    Google Scholar 

  • Ahuja, J. R.: An eye-hair human mosaic. Proc. X. int. Congr. Genetics 1958 II, 2.

    Google Scholar 

  • Allison, A. C.: The distribution of sickle cell trait in East Africa and elsewhere and its apparent relationship to the incidence of subtertian malaria. Trans, roy. Soc. trop. Med. 48, 312–318 (1954) (a).

    Google Scholar 

  • Allison, A. C.: Protection afforded by sickle cell trait against subtertian malaria infection. Brit. med. J. 1954 I, 290 (b).

    Google Scholar 

  • Allison, A. C.: Notes in sickle-cell polymorphism. Ann. hum. Genet. 19, 39–57 (1954) (c).

    Google Scholar 

  • Allison, A. C.: The sickle-cell and haemoglobin C genes in some African populations. Ann. hum. Genet. 21, 67 (1956).

    PubMed  CAS  Google Scholar 

  • Allison, A. C., B. S. B. umberg and W. ap Rees: Haptoglobin types in British, Spanish Basque and Nigerian African populations. Nature (Lond.) 181, 824 (1958).

    Google Scholar 

  • Allison, A. C. and W. ap Rees: The binding of haemoglobin by plasma proteins (haptoglobins). Brit, med. J. 1957 II, 1137.

    CAS  Google Scholar 

  • Allison, A. C. and K.-G. McWhirter: Two unifactorial characters for which man is polymorphic. Nature (Lond.) 1956, 748–749.

    Google Scholar 

  • Allot, E. N., and J. C. Thompson: Familial incidence of low pseudoCholinesterase level. Lancet 1956 II, 517.

    Google Scholar 

  • Anderson, E. P., H. M. Kalckar and K. J. Isselbacher: Defect in uptake of galactose-1- phosphat into liver nucleotides in congenital galactosemia. Science 125, 113–114 (1957) (a).

    Google Scholar 

  • Anderson, E. P., H. M. Kalckar and K. J. Isselbacher: A specific enzymatic defect in congenital galaktosemia. Acta genet. (Basel) 6, 187–188 (1957) (b).

    Google Scholar 

  • Andreassen, M.: Haemofili i Danmark. Op. ex domo biol. hered. Hum. Univ. Hafn. VI. Kopenhagen: Munksgaard 1943.

    Google Scholar 

  • Armstrong, M. D., and K. S. Robinson: On the excretion of indole derivatives in phenylketonuria. Arch. Biochem. 52, 287 (1954).

    PubMed  CAS  Google Scholar 

  • Armstrong, M. D., K. N. F. Shaw and P. E. Wall: The phenolic acids of human urine: Paper chromatography of phenolic acids. J. biol. Chem. 218, 293–303 (1956).

    PubMed  CAS  Google Scholar 

  • Armstrong, M. D. and F. H. Tyler: Studies on phenylketonuria I. Restricted phenylalanine intake in phenylketonuria. J. clin. Invest. 34, 563–580 (1955).

    Google Scholar 

  • Aschner, B. M., and R. H. Post: Modern therapy and hereditary diseases. Acta genet. (Basel) 6, 362–369 (1957).

    CAS  Google Scholar 

  • Atwood, K. C., and S. L. Scheinberg: Somatic variation in human erythrocyte antigens.Symp. on genetic approaches to somatic cell variation. J. cellul. comp. Physiol. 52, Suppl. (1958). Auerbach, C.: A possible case of delayed mutation inman. Ann. hum. Genet. 20, 266–269 (1956).

    Google Scholar 

  • Auerbach, C. and J. M. Robson: Chemical production of mutations. Nature (Lond.) 157, 302 (1946).

    CAS  Google Scholar 

  • Bailey, N. T. J.: The estimation of the frequencies of recessives with incomplete multiple selection. Ann. Eugen. (Lond.) 16, 214–222 (1951–52) (a).

    Google Scholar 

  • Bailey, N. T. J.: A classification of methods of ascertainment and analysis in estmating the frequencies of recessives in man. Ann. Eugen. (Lond.) 16, 223–225, (1951–52) (b).

    Google Scholar 

  • Balme, R. H., and D. Jennings: Gastric ulcer and the ABO blood-groups. Lancet 1957 I, 1219–1220.

    Google Scholar 

  • Baron, J. B., C. E. Dent, H. Harris, E. W. Hart and J. B. Jepson: Hereditary pellagralike skin rash with temporary cerebellar ataxia, constant renal aminoaciduria and other bizarre biochemical features. Lancet 1956, 421–428.

    Google Scholar 

  • Beadle, G. W.: Biochemical genetics. Chem. Rev. 37, 15–96 (1945).

    CAS  Google Scholar 

  • Beadle, G. W. and B. Ephrussi: The differentiation of eye pigments in drosophila as studied by transplantation. Genetics 21, 225–247 (1936).

    PubMed  CAS  Google Scholar 

  • Beadle, G. W. and E. L. Tatum: Genetic control of biochemical reactions in Neurospora. Proc. nat. Acad. Sci. (Wash.) 27, 499–506 (1941).

    CAS  Google Scholar 

  • Bearn, A. G.: Genetic and biochemical aspects of Wilson’s disease. Amer. J. Med. 15, 442–449 (1953).

    PubMed  CAS  Google Scholar 

  • Bearn, A. G.: Wilson’s disease: Is the primary inherited defect one of copper or aminoacid metabolism ? Acta genet. (Basel) 7, 177–178 (1957).

    Google Scholar 

  • Bearn, A. G. and H. G. Kunkel: Wilson’s disease. Ergebn. inn. Med. Kinderheilk. 7, 147–169 (1956).

    CAS  Google Scholar 

  • Becker, P. E.: Dystrophia musculorum progressiva. Stuttgart 1953.

    Google Scholar 

  • Becker, P. E.: Häufigkeit und Bedeutung von Mutationen beim Menschen. Verh. dtsch. Ges. inn. Med. 64, 255–261 (1958).

    Google Scholar 

  • Becker, P. E. u. F. Lenz: Zur Schätzung der Mutationsrate der Muskeldystrophien. Z. menschl. Vererb.- u. Konstit.-Lehre 33, 42–56 (1955).

    CAS  Google Scholar 

  • Becker, P. E. u. F. Lenz: Nachtrag zu der Arbeit “Zur Schätzung der Mutationsrate der Muskeldystrophien.” Z. menschl. Vererb.- u. Konstit.-Lehre. 33, 463–464 (1956).

    Google Scholar 

  • Bell, J.: Dystrophia myotonica and allied diseases. Treas. Hum. Inher. IV, Teil V (1947).

    Google Scholar 

  • Bennhold, H.: Kongenitale Defektdysproteinämien. Verh. dtsch. Ges. inn. Med. 1956, 657–667.

    Google Scholar 

  • Bennhold, H., H. Peters U. E. Roth: Über einen Fall von kompletter Analbuminämie ohne wesentliche klinische Krankheitszeichen. Verh. dtsch. Ges. inn. Med. 1954, 630–634.

    Google Scholar 

  • Benzer, S., V. N. Ingram and H. Lehmann: Three varieties of human haemoglobin D. Nature (Lond.) 182, 852–854 (1958).

    CAS  Google Scholar 

  • Bernheim, F., and M. L. C. Bernheim: The hydrolysis of homatropine and atropine by various tissues. J. Pharmacol, exp. Ther. 64, 209–216 (1938).

    CAS  Google Scholar 

  • Berry, H. K.: Paper chromatographic method for estimating of Phenylalanin. Proc. Soc. exp. Biol. (N. Y.) 95, 71–73 (1957).

    CAS  Google Scholar 

  • Beutler, E.: Glutathione instability of drug sensitive red cells. J. Lab. clin. Med. 49, 84–95 (1957).

    PubMed  CAS  Google Scholar 

  • Beutler, E., R. J. Dern and C. L. Flanagan: Effect of sickle-cell trait on resistance to malaria. Brit, med. J. 1955 I, 1189–1191.

    Google Scholar 

  • Beutler, E., R. J. Dern and A. S. Alving: Hemolytic effect of primaquine. J. Lab. clin. Med. 45, 40–50 (1955) (a).

    Google Scholar 

  • Beutler, E., R. J. Dern, C. L. Flanagan and A. S. Alving: Hemolytic effect of primaquine. J. Lab. clin. Med. 45, 286–295 (1955) (b).

    Google Scholar 

  • Bickel, H.: Papierchromatographische Untersuchungen am Urin und Plasma bei Cystinspeicherkrankheit. Z. Kinderheilk. 72, 15–20 (1952).

    PubMed  CAS  Google Scholar 

  • Bickel, H.: Über einige Aminoacidurien des Kindesalters. Mschr. Kinderheilk. 101, 200 (1953) (a).

    Google Scholar 

  • Bickel, H.: Influence of phenylalanine intake on phenylketonuria. Lancet 1953 II, 812 (b).

    Google Scholar 

  • Bickel, H.: The influence of phenylalanine intake on the chemistry and behaviour of a phenylketonurie child. Acta paediat. (Uppsala) 43, 64 (1954).

    CAS  Google Scholar 

  • Bickel, H.: Zur Biochemie der Wilsonschen Erkrankung. Verh. dtsch. Ges. inn. Med. 61, 402–405 (1955).

    Google Scholar 

  • Bickel, H.: Metabolisch-genetischer Schwachsinn. Verh. dtsch. Ges. inn. Med. 64, 249–251 (1958).

    Google Scholar 

  • Block, R. J., E. L. Durrum and G. Zweig: A manual of paper chromatography and paper electrophoresis. New York: Acad. Press. Inc. 1955.

    Google Scholar 

  • Block, W. D., J. G. Rukavina and A. C. Curtis: Serum electrophoretic studies on patients with familial primary systemic amyloidosis. J. Lab. clin. Med. 47, 357–364 (1956).

    PubMed  CAS  Google Scholar 

  • Bodanski, O.: Methemoglobinemia and methemoglobin producing compounds. Pharmacol. Rev. 3, 144–196 (1956).

    Google Scholar 

  • Böök, J. A.: Schizophrenia as a gene mutation. Acta genet. (Basel) 4, 43 (1953).

    Google Scholar 

  • Böök, J. A.: Genetical investigations in a North Swedish population. Ann. hum. Genet. 21, 191–221 (1957).

    PubMed  Google Scholar 

  • Böök, J. A. and R. Kostmann: Prospects of biochemical genetics in medicine. Ann. hum. Genet. 20, 251–253 (1956).

    PubMed  Google Scholar 

  • Boggs, J. D., D. Yi-Yung Hsia, R. S. Mais and J. A. Bigler: Genetic mechanism of idiopathic hyperlipemia. N. Engl. J. Med. 257, 1101–1108 (1957).

    PubMed  CAS  Google Scholar 

  • Bonner, D. M.: Gene-enzyme relationships in neurospora. Cold Spr. Harb. Symp. quant. Biol. 16, 143–157 (1951).

    CAS  Google Scholar 

  • Borberg, A.: Clinical and genetic investigations into tuberous sclerosis and Recklinghausen’s neurofibromatosis. Kopenhagen 1951.

    Google Scholar 

  • Brage, D.: Hepatolenticular syndrome and familial hyperaminoaciduria: The expression of homozygotes and heterozygotes. Proc. X. int. Congr. Genet. 1958 II, 31–32.

    Google Scholar 

  • Brinkhous, K. M., and J. B. Graham: Hemophilia and the hemophilioid states. Blood 9, 254–257 (1954).

    PubMed  CAS  Google Scholar 

  • Browne, E. A.: The inheritance of an intrinsic abnormality of the red blood cell predisposing to drug-induced hemolytic anemia. Bull. John Hopk. Hosp. 101, 115 (1957).

    Google Scholar 

  • Bruton, O. C.: Agammaglobulinemia. Pediatrics 9, 722–728 (1952).

    PubMed  CAS  Google Scholar 

  • Butenandt, A.: Biochemie der Gene und Genwirkungen. Naturwissenschaften 40, 91–100 (1953).

    CAS  Google Scholar 

  • Campbell, A. M., and S. Spiegelman: The growth kinetics of elements necessary for galactozymase formation in “long term adapting” yeasts. C. R. Lab. Carlsberg, Ser. physiol. 26, 13–30 (1956).

    CAS  Google Scholar 

  • Carson, P. E., C. L. Flanagan, C. E. Ickes and A. S. Alving: Enzymatic deficiency in primaquine-sensitive erythrocytes. Science 124, 484–485 (1956).

    PubMed  CAS  Google Scholar 

  • Ceppellini, R., L. C. Dunn and M. Turri: An interaction between alleles at the Rh locus in man which weakens the reactivity of the Rh0 factor (Du). Proc. nat. Acad. Sci. (Wash.) 41, 283–288 (1955).

    CAS  Google Scholar 

  • Ceppellini, R., e M. Siniscalco: Una nuova impotesi genetica per il sistema Lewis-secretore e suoi riflessi nei riguardi di alcune evidenze di linkage con altri loci. Riv. 1st. sieroter. ital. 30, 431–445 (1955).

    CAS  Google Scholar 

  • Chalmers, J. N. M., and S. D. Lawler: Data on linkage in man: Elliptocytosis and blood groups. 1. Families 1 and 2. Ann. Eugen. (Lond.) 17, 267–271 (1953).

    CAS  Google Scholar 

  • Chase, H. B.: Inheritance and selection of insulin-resistance in mice. Genetics 35, 101 (1950).

    Google Scholar 

  • Cheeseman, E. A., S. J. Kilkpatrick, A. C. Stevenson and C. A. B. Smith: The sex ratio of mutation rates of the sex-linked recessive genes in man with particular reference to Duchenne type muscular dystrophy. Ann. hum. Genet. 22, 235–263 (1958).

    PubMed  CAS  Google Scholar 

  • Chu, E. H. Y., and N. H. Giles: Chromosome complements and nucleoli in normal human somatic cells in culture. Proc. X. int. Congr. Genet. 1958 II, 50.

    Google Scholar 

  • Clarke, C. A., and P. M. Sheppard: The ABO blood groups in duodenal ulcer. A study of sibships. Acta genet. (Basel) 6, 570–574 (1957).

    CAS  Google Scholar 

  • Clarke, C. A., and P. M. Sheppard: Disease in relation to human polymorphic systems. Proc. X. int. Congr. Genet. 1958 II, 52.

    Google Scholar 

  • Codounis, A.: A genetical study on the “hereditary methaemoglobinaemic cyanosis”. Acta genet. (Basel) 6, 131–140 (1957).

    Google Scholar 

  • Cramer, F.: Papierchromatographie 3. Aufl. Weinheim: Verlag Chemie 1954.

    Google Scholar 

  • Crowe, F. W., W. J. Schull and J. V. Neel: A clinical, pathological, and genetic study of multiple neurofibromatosis. Springfield, I11. USA 1956.

    Google Scholar 

  • Crumpler, H. R., C. E. Dent, H. Harris and R. G. Westall: ß-aminobutyric acid (α-methyl- ß -alanin): a new amino-acid obtained from human urine. Nature (Lond.) 167, 307 (1951).

    CAS  Google Scholar 

  • Dalgaard, O. Z.: Bilateral polycystic disease of the kidneys. Opera ex domo 38, 255 pp. Kopenhagen: Munksgaard 1957.

    Google Scholar 

  • Danforth, G. H.: The frequency of mutation and the incidence of hereditary traits in man. Eugenics, Genetics and the Family. Sc. Papers 2nd Internat. Congr. Eugen. N. Y. 1921, 1, p. 120–128.

    Google Scholar 

  • Debrisk, A. G.: Metabolic aspects of chemical genetics. Advanc. Enzymol. 17, 393–476 (1956).

    Google Scholar 

  • Delijannis, G. A.: Über das Auftreten der Sichelzellkrankheit in Griechenland. Blut 2, 241–247 (1956).

    PubMed  CAS  Google Scholar 

  • Demerec, M.: What is a gene ? — Twenty years later. Amer. Naturalist 89, 5–20 (1955).

    Google Scholar 

  • Dent, C. E.: The amino-aciduria in Fanconi syndrome. A study making extensive use of techniques based on paper partition chromatography. Biochem. J. 41, 240 (1947).

    CAS  Google Scholar 

  • Dent, C. E. and G. R. Philpott: Xanthinuria, an inborn error (or deviation) of metabolism. Lancet 1954 I, 182–185.

    Google Scholar 

  • Dent, C. E. and H. Harris: The genetics of cystinuria. Ann. Eugen. (Lond.) 16, 60–87 (1951–52).

    Google Scholar 

  • Dent, C. E. and A. G. Rose: Amino-acid metabolism in cystinuria. Quart. J. Med. N. S. 20, 205 (1951).

    CAS  Google Scholar 

  • Deutsch, E.: Die hämophilie-ähnlichen hämorrhagischen Diathesen. Ergebn. inn. Med. Kinderheilk. N. F. 5, 553–641 (1954).

    CAS  Google Scholar 

  • Deutsch, E.: Blutgerinnungsfaktoren. Einzeldarstellungen aus dem Gesamtgebiet der Biochemie. Neue Folge, Bd. 1. Wien 1955.

    Google Scholar 

  • Dobzhansky, Th.: Genetics and the origin of species. 3rd. Ed. New York: Columbia Univ. Press 1951.

    Google Scholar 

  • Duis, B. T.: Zwillingskatamnesen. Klinische Befunde bei Nachuntersuchung einer auslesefreien Zwillingsserie. Acta genet, med. (Roma) 5, 14–103 (1956).

    CAS  Google Scholar 

  • Dukes, L. E.: Familial intestinal polyposis. Ann. Eugen. (Lond.) 17, 1—29 (1952—53).

    Google Scholar 

  • Eder, H. A., C. Finch and R. W. McKee: Congenital methemoglobinemia. A clinical and biochemical study of a case. J. clin. Invest. 28, 265 (1949).

    CAS  Google Scholar 

  • Ehling, U.: Untersuchungen zur kausalen Genese erblicher Katarakte beim Kaninchen. Z. menschl. Vererb.- u. Konstit.-Lehre 34, 77–104 (1957).

    CAS  Google Scholar 

  • Ehrenberg, L., G. v. Ehrenstein and A. Hedgran: Gonad temperature and spontaneous mutation rate in man. Nature (Lond.) 180, 1433–1434 (1957).

    CAS  Google Scholar 

  • Eisenberg, F. jr., K. J. Isselbacher and H. M. Kalckar: Studies on metabolism of carbon- 14-labeled galactose in a galactosemic individual. Science 125, 116–117 (1957).

    PubMed  CAS  Google Scholar 

  • Elphistone, R. H., I. G. Wickes and A. B. Anderson: Familial agammaglobulinaemia. Brit. med. J. 1956 II, 336–338.

    Google Scholar 

  • Ephrussi, B., and H. Hottinguer: Cytoplasmic constituents of heredity. Cold Spr. Harb. Symp. quant. Biol. 16, 75–85 (1951).

    CAS  Google Scholar 

  • Finney, D. J.: The detection of linkage. Ann. Eugen. (Lond.) 10, 171–214 (1940).

    Google Scholar 

  • Finney, D. J.: The detection of linkage. 4. Lack of parental records and the use of empirical estimates of information. J. Hered. 33, 157–160 (1941).

    Google Scholar 

  • Finney, D. J.: The detection of linkage. 2. Further mating types; scoring for Boyd’s data. Ann. Eugen. (Lond.) 11, 10–30 (1941–42).

    Google Scholar 

  • Finney, D. J.: The detection of linkage. 3. Incomplete parental testing. Ann. Eugen. (Lond.) 11, 115–135 (1941–42).

    Google Scholar 

  • Finney, D. J.: The detection of linkage. 5. Supplementary tables. Ann. Eugen. (Lond.) 11, 224–232 (1941–42).

    Google Scholar 

  • Finney, D. J.: The detection of linkage. 6. The loss of information from incompleteness of parental records. Ann. Eugen. (Lond.) 11, 233–244 (1941–42).

    Google Scholar 

  • Finney, D. J.: The detection of linkage. 7. Combination of data from matings of known and unknown phase. Ann. Eugen. (Lond.) 12, 31–43 (1943).

    Google Scholar 

  • Finney, D. J.: The truncated binomial distribution. Ann. Eugen. (Lond.) 14, 319–328 (1947–49).

    Google Scholar 

  • Fleischhacker, H.: Mutationen im ABO-System ? Anthrop. Anz. 20, 271–282 (1957).

    Google Scholar 

  • Fonio, A.: Die erblichen und die sporadischen Bluterstämme in der Schweiz. Basel 1954.

    Google Scholar 

  • Ford, C. E., and J. L. Hamerton: The chromosomes of man. Acta genet. (Basel) 6, 264–266 (1957)

    Google Scholar 

  • Ford, E. B.: Polymorphism. Biol. Rev. 20, 73–88 (1945).

    Google Scholar 

  • Franceschetti, A., et D. Klein: Le dépistage des hétérozygotes. Genetica med. Ed. L. Gedda. Rom 1954, p. 50–78.

    Google Scholar 

  • Fraser Roberts, J. A.: Association between blood groups and disease. Acta genet. (Basel) 6, 549–560 (1957) (a).

    Google Scholar 

  • Fraser Roberts, J. A.: ABO blood groups and duodenal ulcer. Brit. med. J. 1957 I, 758–759 (b).

    Google Scholar 

  • Fraser Roberts, J. A.: Some further observations on associations between blood groups and disease. Proc. X. int. Congr. Genet. 1958 II, 237–238.

    Google Scholar 

  • Freudenberg, E.: Cystinosis. Ergebn. inn. Med. Kinderheilk. 10, 481–511 (1958).

    CAS  Google Scholar 

  • Frosch, E. R., A. Prader, A. Labhart, H. W. Stuber u. H. P. Wolf: Hereditäre Fructose- intoleranz, eine bisher nicht bekannte kongenitale Stoffwechselstörung. Schweiz, med. Wschr. 1957, 1168.

    Google Scholar 

  • Galatius-Jensen, F.: Electrophoretic pattern of hereditary human serum proteins. Acta genet. (Basel) 6, 516–517 (1957).

    CAS  Google Scholar 

  • Gartler, S. M.: An investigation into the biochemical genetics of ß-aminoisobutyric aciduria. Proc. X. int. Congr. Genet. 1958 II, 94.

    Google Scholar 

  • Gartler, S. M., I. L. Firscheim and B. Kraus: An investigation into the genetics and racial variation of Baib excretion. Amer. J. hum. Genet. 9, 200–207 (1957).

    PubMed  CAS  Google Scholar 

  • Gates, R. R.: Records of Y-inherited hairy ears in India. Acta genet, med. (Roma) 6, 103–108 (1957).

    CAS  Google Scholar 

  • Gedda, L.: Studio dei gemelli. Rom 1951.

    Google Scholar 

  • Gerald, P. S., and L. K. Diamond: Evidence for an etiologic differentiation of dominantly and recessively transmitted methemoglobinemic cyanosis. Proc. X. int. Congr. Genet. 1958 II, 94–95.

    Google Scholar 

  • Gibson, R. H.: The reduction of methaemoglobin in red blood cells and studies on cause of idiopathic methaemoglobinaemia. Biochem. J. 42, 13 (1948).

    CAS  Google Scholar 

  • Gibson, R. H. and D. C. Harrison: Familial idiopathic methaemoglobinaemia. Lancet 1947 II, 941. Glick, D. S., and S. Glaubach: The occurence and distribution of atropinesterase, and the specifity of tropinesterases. J. gen. Physiol. 25, 197 (1941).

    Google Scholar 

  • Goldschmidt, R. B.: Theoretical Genetics. Berkeley and Los Angeles: Univ. of. California Press. 1955.

    Google Scholar 

  • Goodall, H. B., D. W. Hendry, S. D. Lawler and S. A. Stephen: Data on linkage in man: elliptocytosis and blood groups. 2. Family 3. Ann. Eugen. (Lond.) 17, 272–278 (1953).

    CAS  Google Scholar 

  • Goodall, H. B., D. W. Hendry, S. D. Lawler and S. A. Stephen: Data on linkage in man: elliptocytosis and blood groups. 3. Family 4. Ann. Eugen. (Lond.) 18, 325–327 (1954).

    CAS  Google Scholar 

  • Goodman, H. O., and S. C. Reed: Heredity of fibrosis of the pancreas. Possible mutation rate of the gene. Amer. J. hum. Genet. 4, 59–71 (1952).

    PubMed  CAS  Google Scholar 

  • Graham, J. B.: Biochemical genetics of blood coagulation. Amer. J. hum. Genet. 8, 63–79 (1956).

    PubMed  CAS  Google Scholar 

  • Graham, J. B. and C. E. Badgley: Split-hand with unusual complications. Amer. J. hum. Genet. 7, 44 (1955).

    PubMed  CAS  Google Scholar 

  • Grebe, H.: Chondrodysplasie. Analecta genet. Rom 1955.

    Google Scholar 

  • Grebe, H.: Die Akrocephalosyndaktylie. Z. menschl. Vererb.- u. Konstit.-Lehre 28, 209–261 (1944).

    Google Scholar 

  • Grebe, H.: Diskordanzursachen bei erbgleichen Zwillingen. Acta Genet, med. (Roma) 1, 89–102 (1952).

    CAS  Google Scholar 

  • Grouchy, J. de, and H. E. Sutton: A genetic study of aminoisobutyric acid excretion. Amer. J. hum. Genet. 9, 76–80 (1957).

    Google Scholar 

  • Grubb, R.: A relationship between blood group serology and rheumatoid arthritis serology. Serum protein groups. Vox Sang. (Basel) 2, 305–312 (1957).

    CAS  Google Scholar 

  • Grüttner, R.: Die Oligophrenia phenylpyruvica. Dtsch. med. Wschr. 1957, 155–156.

    Google Scholar 

  • Gunther, M., and L. S. Penrose: The genetics of epiloia. J. Genet. 31, 413–430 (1935).

    Google Scholar 

  • Hadorn, E.: Letalfaktoren in ihrer Bedeutung für Erbpathologie und Genphysiologie der Entwicklung. Stuttgart 1955.

    Google Scholar 

  • Hadorn, J., and H. Niggli: Mutations in drosophila after chemical treatment of gonads in vitro. Nature (Lond.) 157, 162–163 (1946).

    CAS  Google Scholar 

  • Haecker, V.: Entwicklungsgeschichtliche Eigenschaftsanalyse (Phänogenetik). Jena 1918.

    Google Scholar 

  • Haldane, J. B. S.: The rate of spontaneous mutation of a human gene. J. Genet. 31, 317–326 (1935).

    Google Scholar 

  • Haldane, J. B. S.: A search for incomplete sex linkage in man. Ann. Eugen. (Lond.) 7, 28–57 (1936).

    Google Scholar 

  • Haldane, J. B. S.: A probable new sex-linked dominant in man. J. Hered. 28, 58–60 (1937).

    Google Scholar 

  • Haldane, J. B. S.: The spread od harmful autosomal recessive genes in human populations. Ann. Eugen. (Lond.) 9, 232–237 (1939).

    Google Scholar 

  • Haldane, J. B. S.: The mutation rate of the gene for haemophilia, and its segregation ratios in males and females. Ann. Eugen. (Lond.) 13, 262–271 (1947).

    CAS  Google Scholar 

  • Haldane, J. B. S.: The rate of mutation of human genes. Proc. VIII, Internat. Congr. Genet. Stockholm 1948, 267–273.

    Google Scholar 

  • Haldane, J. B. S.: The biochemistry of genetics. London 1954.

    Google Scholar 

  • Haldane, J. B. S.: Mutation in sex-linked recessive type of muscular dystrophy. A possible sex difference. Ann. hum. Genet. 20, 344–347 (1956).

    PubMed  CAS  Google Scholar 

  • Haldane, J. B. S. and U. Philip: The daughters and sisters of haemophilics: J. Genet. 38, 193–200 (1939).

    Google Scholar 

  • Haldane, J. B. S. and C. A. B. Smith: A new estimate of the linkage between the genes for colour blindness and haemophilia in man. Ann. Eugen. (Lond.) 14, 10–31 (1947).

    CAS  Google Scholar 

  • Hanhart, E.: Über 27 Sippen mit infantiler amaurotischer Idiotie (Tay-Sachs). Acta genet, med. (Roma) 3, 331–364 (1954).

    Google Scholar 

  • Hanhart, E. and M. Fraccaro: A pedigree with 96 cases of incompete dominant X-chromosomal nystagmus. Proc. 9th int. Cong. Genetics Caryologia, Suppl. VI, p 1248, 1954.

    Google Scholar 

  • Harris, H.: A sex-limiting modifying gene in diaphysial aclasis (multiple exostoses). Ann. Eugen. (Lond.) 14, 165–170 (1947–49).

    Google Scholar 

  • Harris, H.: An introduction to human biochemical genetics. Eugen. Lab. Mem. XXXVII. London 1953.

    Google Scholar 

  • Harris, H.: Genes and enzymes in man. Novant’ anni delle leggi mendeliane. Rom 1956.

    Google Scholar 

  • Harris, H.: Family studies on the urinary excretion of ß-aminoisobutyric acid. Ann. hum. Genet. 18, 43–49 (1953–54).

    Google Scholar 

  • Harris, H.,U. Mittwoch, E. B. Robson, and F. C. Warren: Phenotypes and genotypes in cystinuria. Ann. hum. Genet. 20, 57–91 (1955).

    Google Scholar 

  • Harris, H. and E. B. Robson: The genetics of hypophosphatasia: The excretion of ethanolamine phosphate in clinically normal relatives. Proc. X. int. Congr. Genetics 1958 II, 113–114.

    Google Scholar 

  • Harris, H. andF. L. Warren: Quantitative studies on the urinary cystine in patients with cystine stone formation and in their relatives. Ann. Eugen. (Lond.) 18, 125–174 (1953–54).

    Google Scholar 

  • Harris, R. C., and C. Olmo: Liver and kidney glucose-6-phosphatase activity in childhood with normal and diseased organs. J. clin. Invest. 33, 1204–1209 (1954).

    PubMed  CAS  Google Scholar 

  • Harvald, B., and M. Hauge: A catamnestic investigation of Danish twins. Dan. med. Bull. 3, 150–158 (1956).

    PubMed  CAS  Google Scholar 

  • Hawthorne, D. C.: The genetics of galactose fermentation in saccharomyces hybrids. C. R. Lab. Carlsberg, Sér. physiol. 26, 149–160 (1956).

    Google Scholar 

  • Helmbold, W.: Über den Zusammenhang zwischen ABO-Blutgruppen und weiblichem Genital-Ca. Kongress int. Ges. Bluttransf. Rom 1958.

    Google Scholar 

  • Helmbold, W.: Über den Zusammenhang zwischen ABO-Blutgruppen und Krankheiten. Blut 5 (1959) (im Druck).

    Google Scholar 

  • Henderson, W.: A case of hartnup disease. Arch. Dis. Childh. 33, 114 (1958).

    PubMed  CAS  Google Scholar 

  • Heuchel, G., u. D. Jorke: Über die Gammaglobulin-Mangelkrankheit. Medizinische 1955, 1181–1186.

    Google Scholar 

  • Hockwald, R. S., J. Arnold, C. B. Clayman and A. S. Alving: Toxity of primaquine in Negroes. J. Amer. med. Ass. 149, 1568–1570 (1952).

    CAS  Google Scholar 

  • Holzel, A., and G. Komrower: A study of the genetics of galactosaemia. Arch. Dis. Childh. 30, 155–159 (1955).

    PubMed  CAS  Google Scholar 

  • Homburger, H., and M. L. Petermann: Studies on hypoproteinemia. II Familial idiopathic dysproteinemia. Blood 4, 1085–1108 (1949).

    PubMed  CAS  Google Scholar 

  • Hörlein, H., u. G. Weber: Über chronische familiäre Methämoglobinämie und eine neue Modifikation des Methämoglobins. Dtsch. med. Wschr. 1948, 476.

    Google Scholar 

  • Horowitz, N. H.: Biochemical genetics of neurospora. Advanc. Genet. 3, 33–71 (1950).

    CAS  Google Scholar 

  • Horowitz, N. H. and S.-C. Sheng: Neurospora Tyrosinase. J. biol. Chem. 197, 513–520 (1952).

    CAS  Google Scholar 

  • Horsfall, W. R., and O. Smithies: Genetic control of some human serum ß-globulins. Science 128, 35 (1958).

    PubMed  CAS  Google Scholar 

  • Hsia, D. Y.: The laboratory detection of heterozygotes. Amer. J. human Genet. 9, 98–116 (1957).

    CAS  Google Scholar 

  • Hsia, D. Yi-Yung, K. Driscoll, W. Troll and W. E. Knox: Heterozygous carriers of phenylketonuria detected by phenylalanine tolerance tests. Acta genet. (Basel) 7, 189–190 (1957).

    Google Scholar 

  • Hsia, D. Yi-Yung, W. E. Knox, K. V. Quinn and R. S. Paine: A one-year, controlled study of the effect of low-phenylalanine diet on phenylketonuria. Pediatrics 21, 178–202 (1958).

    PubMed  CAS  Google Scholar 

  • Hsu, T. C., and C. M. Pomerat: Mammalian chromosomes in vitro. J. Hered. 44, 23–29 (1953).

    Google Scholar 

  • Illingworth, B., and G. T. Cori: Structure of glycogens and amylopectins. III. Normal and abnormal human glycogen. J. biol. Chem. 199, 653–660 (1952).

    PubMed  CAS  Google Scholar 

  • Ingram, V. M.: Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin. Nature (Lond.) 180, 325–328 (1957).

    Google Scholar 

  • Ingram, V. M. and J. A. Hunt: Allelmorphism and the chemical differences of the human haemoglobins A, S and C. Nature (Lond.) 181, 1062–1063 (1958).

    Google Scholar 

  • Jameson, R. J., S. D. Lawler and J. H. Renwick: Nail-patella syndrome: Clinical and linkage data of family G. Ann. hum. Genet. 20, 348–353 (1956).

    PubMed  CAS  Google Scholar 

  • Juel-Nielsen, N., and A. Mogensen: Uniovular twins brought up apart. Acta genet. (Basel) 7, 430–433 (1957).

    CAS  Google Scholar 

  • Juel-Nielsen, N. and B. Harvald: The electroencephalogram in uniovular twins brought up apart. Acta genet. (Basel) 8, 57–64 (1958).

    CAS  Google Scholar 

  • Kaelin, A.: Statistische Prüf- und Schätzverfahren für die relative Häufigkeit von Merkmalsträgern in Geschwisterreihen bei einem der Auslese unterworfenen Merkmal mit Anwendung auf das Retinagliom. Arch. Klaus-Stift. Vererb.-Forsch. 30, 263–485 (1955).

    Google Scholar 

  • Kalckar, H. M.: Biochemical mutations in man and microorganism. Science 125, 105–108 (1957).

    PubMed  CAS  Google Scholar 

  • Kalow, W.: Familial incidence of low pseudoCholinesterase level. Lancet 1956 II, 576–577.

    Google Scholar 

  • Kapila, C. C., S. Kaul and B. C. Chatterjee: Glycogen storage of liver. Brit. med. J. 1956 I, 893–895.

    Google Scholar 

  • Kempthorne, O.: An introduction to genetic statistics. New York: John Wiley & Sons 1957.

    Google Scholar 

  • Kimbro, F. I., M. Sachs and J. V. Tobert jun.: Mechanism of hemolytic anemia induced by nitrofurantoin (furadantin). Fed. Proc. 16, 312 (1957).

    Google Scholar 

  • Klein, D.: Metabolic disorders. In: A. Sorsby (Ed) clinical genetics. London: Butterworth & Co 1953.

    Google Scholar 

  • Klein, D.: La dystrophic myotonique (Steinert) et la myotome congénitale (Thomsen) en Suisse. J. Génét. hum. 7, Suppl. (1958).

    Google Scholar 

  • Knedel, M.: Die Doppel-Albuminämie, eine neue erbliche Proteinanomalie. Blut 3, 129–134 (1957).

    PubMed  CAS  Google Scholar 

  • Knox, W. E.: Sir Archibald Garrod’s “inborn error of metabolism” 1. Cystinuria, 2. Alkaptonuria, 3. Albinism, 4. Pentosuria. Amer. J. hum. Genet. 10, 3–32, 95–124, 249–267, 385–397 (1958).

    Google Scholar 

  • Koch, G.: Ergebnisse aus den Nachuntersuchungen der Berliner Zwillingsserie nach 20–25 Jahren (Vorläufige Ergebnisse). Acta genet. (Basel) 7, 47–52 (1957).

    CAS  Google Scholar 

  • Koch, G.: Interne Befunde aus der Nachuntersuchung der Berliner Zwillingsserie nach 20–25 Jahren. Verh. dtsch. Ges. inn. Med. 64, 273–277 (1958).

    Google Scholar 

  • Kodani, M.: The diploid chromosome numbers of man. Proc. nat. Acad. Sci. (Wash.) 43, 286–292 (1957).

    Google Scholar 

  • Koller, S.: Methodik der menschlichen Erbforschung. Handbuch der Erbbiologie des Menschen. Bd. 2, S. 249–309, 1940.

    Google Scholar 

  • Kostmann, R.: Infantile genetic agranulocytosis. Acta paediat. (Uppsala) Suppl. 105 (1956).

    Google Scholar 

  • Krooth, R. S.: The use of the fertilities of affected individuals and their unaffected sibs in the estimation of fitness. Amer. J. hum. Genet. 7, 325–360 (1955).

    PubMed  CAS  Google Scholar 

  • Krooth, R. S.: On the estimation of the frequency of genetic carriers. Amer. J. hum. Genet. 9, 170–180 (1957).

    PubMed  CAS  Google Scholar 

  • Kubahashi, K.: Enzyme formation in galactose-negative mutants of Escherichia coli. Science 125, 114–116 (1957).

    Google Scholar 

  • Kühn, A.: Über eine Gen-Wirkkette der Pigmentbildung bei Insekten. Nachr. Ges. Wiss. Göttingen, Math.-Phys. Kl. 6, 231–261 (1941).

    Google Scholar 

  • Kühn, A.: Vorlesungen über Entwicklungsphysiologie. Berlin-Göttingen-Heidelberg: Springer 1955.

    Google Scholar 

  • Kühn, A.: Versuche zur Entwicklung eines Modells der Genwirkungen. Naturwissenschaften 43, 25–28 (1956).

    Google Scholar 

  • Landauer, W. and A.: Chick mortality and sex-ratio in the domestic fowl. Amer. Naturalist 65, 492–501 (1931).

    Google Scholar 

  • Langmann, H.: Ein Beitrag zur Frage der Beziehungen zwischen Blutgruppen und weiblichen Genital- und Mamma-Carcinom. Diss. Bonn 1955.

    Google Scholar 

  • Lawler, S. D.: Family studies showing linkage between elliptocytosis and the Rhesus blood group system. Proc. IX int. Congr. of Genet. Caryologia Suppl. (1955).

    Google Scholar 

  • Lawler, S. D., J. H. Renwick and L. S. Wildervanck: Further families showing linkage between the ABO and nail-patella loci, with no evidence of heterogeneity. Ann. hum. Genet. 21,410–419(1956–57).

    Google Scholar 

  • Lawler, S. D. and M. Sandler: Data on linkage in man: Elliptocytosis and blood groups. 4. Families 5, 6, and 7. Ann. Eugen. (Lond.) 18, 328–334 (1954).

    CAS  Google Scholar 

  • Lehmann, H.: Distribution of abnormal haemoglobins. J. clin. Path. 9, 180–181 (1956).

    Google Scholar 

  • Lehmann, H.: Variations of haemoglobin synthesis in man. Acta genet. (Basel) 6, 413–429 (1957).

    CAS  Google Scholar 

  • Lehmann, H. and M. Cutbush: Sickle cell trait in Southern India. Brit. med. J. 1952 I, 404.

    Google Scholar 

  • Lehmann, H. and A. B. Raper: Maintenance of high sickling rate in an African community. Brit. med. J. 1956, 333–336.

    Google Scholar 

  • Lehmann, H. and E. Ryan: Familial incidence of low pseudoCholinesterase level. Lancet 1956 II, 124.

    Google Scholar 

  • Lehmann, W.: Bemerkung zur Genetik der hämorrhagischen Diathesen. “Hämorrhagische Diathesen” Internat. Symposium, Wien 4./5. 2. 55, S. 114–119.

    Google Scholar 

  • Lehmann, W.: Erbliche — plasmatische und thrombocytogene Gierinnungsstörungen. Verh. dtsch. Ges. inn. Med. 65, 213–225 (1958).

    Google Scholar 

  • Lejeune, J., et R. Turpin: Mutations radio-induites chez l’homme et dose de doublement Sur la validité d’une estimation directe. Acad. franç. Sci. 1957, 2425–2426.

    Google Scholar 

  • Lejeune, J.,et R. Turpin, M. O. Rethore: Sur les variations de la masculinité dans la descendance des parents irradiés. Proc. X. int. Congr. Genet. 1958 II, 163.

    Google Scholar 

  • Lennox, W. G., E. L. Gibbs and F. A. Gibbs: The brain wave pattern, an hereditary trait. J. Hered. 36, 233–243 (1943).

    Google Scholar 

  • Lenz, F.: Über die Häufigkeit und Bedeutung von Mutationen in menschlichen Populationen. Homo 3, 145–148 (1952).

    Google Scholar 

  • Lenz, F.: Diskussionsbemerkung. Acta genet. (Basel) 7, 489 (1957).

    Google Scholar 

  • Lenz, W.: Die Bedeutung des Alters der Eltern für den Zwergwuchs. Ann. hum. Genet. 22, 44–57 (1957).

    PubMed  CAS  Google Scholar 

  • Lerner, A. B.: Metabolism of phenylalanine and tyrosine. Ad vane. Enzymol. 14, 73–128 (1953).

    CAS  Google Scholar 

  • Lerner, I. M.: Population genetics and animal improvement. Cambridge Univ. Press 1950.

    Google Scholar 

  • Lerner, I. M.: Genetic homeostasis. London: Oliver and Boyd 1954.

    Google Scholar 

  • Levine. P., E. Robinson, M. Celano, O. Briggs and L. Falkinburg: Gene interaction resulting in suppression of blood group substance B. Blood 10, 1100–1108 (1955).

    PubMed  CAS  Google Scholar 

  • Li, C. C.: Population genetics. Chicago 1955.

    Google Scholar 

  • Livingstone, F. B.: Anthropological implications of sickle cell gene distribution in West Africa. Amer. Anthropol. 60, 533–562 (1958).

    Google Scholar 

  • Loeffler, L.: Möglichkeiten und Grenzen der Schätzung der Mutationsrate beim Menschen. Arbeitskreis IV/4 “Strahlenbiologie”. Deutsche Atomkommission.

    Google Scholar 

  • Luder, J., and W. Sheldon: A familiar tubular absorption defect of glucose and amino-acids. Arch. Dis. Childh. 30, 160–164 (1955).

    PubMed  CAS  Google Scholar 

  • Ludwig, W., u. Ch. Boost: Vergleichende Wertung der Methoden zur Analyse recessiver Erbgänge beim Menschen. Z. menschl. Vererb.- u. Konstit.-Lehre 24, 577–619 (1940).

    Google Scholar 

  • Lynas, M. A.: Dystrophia myotonica with special reference to Northern Ireland. Ann. hum. Genet. 21, 318–351 (1956–57).

    Google Scholar 

  • Mackenroth, G.: Bevölkerungslehre. Berlin, Göttingen, Heidelberg: Springer 1953.

    Google Scholar 

  • Mackenzie, H. J., and L. S. Penrose: Two pedigrees of ectrodactyly. Ann. Eugen. (Lond.) 16, 88–96 (1951).

    Google Scholar 

  • Matsunaga, E.: Intra-uterine selection by the ABO incompatibility of mother and foetus. Amer. J. hum. Genet. 7, 66–71 (1955).

    PubMed  CAS  Google Scholar 

  • Matsunaga, E.: Selektion durch Unverträglichkeit im ABO-Blutgruppensystem zwischen Mutter und Fetus. Blut 2, 188–198 (1956).

    PubMed  CAS  Google Scholar 

  • Mayr, E., L. E. Diamond, R. P. Levine and M. Mayr: A suspected correlation between blood group frequency and chromophobe adenoma of the pituitary. Acta genet, statist, med. 6, 580 (1957).

    Google Scholar 

  • McConnell, R. B., and P. M. Sheppard: The secretor character and disease. Acta genet. (Basel) 6, 574–579 (1957).

    CAS  Google Scholar 

  • McElroy, W., and B. Glass (Ed.): The chemical basis of heredity. Baltimore: John Hopkins Press 1957.

    Google Scholar 

  • Medes, G.: A new error of tyrosine metabolism; Tyrosinosis. Biochem. J. 26, 917 (1932).

    CAS  Google Scholar 

  • Messeri, E.: Consideration! ecologiche sul comportamento di due fattori ereditari nell’ uomo. Caryologia 10, 443–49 (1958).

    Google Scholar 

  • Milch, R. A., and H. Milch: Dominant inheritance of alcaptonuria. Acta genet. (Basel) 7, 178 (1957).

    CAS  Google Scholar 

  • Miller, A. A.: Congenital sulfhemoglobinemia. J. Pediat. 51, 233–237 (1957).

    PubMed  CAS  Google Scholar 

  • Mitschrich, H.: Zwillingstuberkulose. III. Stuttgart 1956.

    Google Scholar 

  • Mohr, J.: A study of linkage in man. Op. ex domo biol. Hered. Human. Univ. Hafn. 33. Kopenhagen 1954.

    Google Scholar 

  • Møllenbach, C. J.: Medfødte defekter i ojets indre hinder, Klinik og arvelighedsforhold. Op. ex. domo. biol. Hered. Human. Univ. Hafn. Kopenhagen: Munksgaard 1947.

    Google Scholar 

  • Moor-Jankowski, J. K., G. Truog u. J. J. Huser: Der Bluterstamm von Tenna und seine Nachkommen. Acta genet. (Basel) 7, 597–780 (1957).

    CAS  Google Scholar 

  • Mørch, E. T.: Chondrodystrophic dwarfs in Denmark. Opera ex Domo Biol. Hered. Human. Univ. Hafn. 3, 200 (1941).

    Google Scholar 

  • Morton, N. E.: Sequential tests for the detection of linkage. Amer. J. hum. Genet. 7, 277–318 (1955).

    PubMed  CAS  Google Scholar 

  • Morton, N. E.: The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type. Amer. J. hum. Genet. 8, 80–96 (1956).

    PubMed  CAS  Google Scholar 

  • Morton, N. E.: Further scoring types in sequential tests, with a critical review of autosomal and partial sex linkage in man. Amer. J. hum. Genet. 9, 55–75 (1957).

    PubMed  CAS  Google Scholar 

  • Morton, N. E., J. F. Crow and H. J. Muller: An estimate of the mutational damage in man from data on consanguineous marriages. Proc. nat. Acad. Sci. (Wash.) 42, 855–863 (1956).

    CAS  Google Scholar 

  • Morton, N. E.: Segregation analysis in human genetics. Science 127, 79–80 (1958a).

    PubMed  CAS  Google Scholar 

  • Morton, N. E.: Empirical risks in consanguineous marriages: Birth weight, gestation time, and measurements of infants. Amer. J. hum. Genet. 10, 344–349 (1958b).

    PubMed  CAS  Google Scholar 

  • Motulsky, A. G.: Drug reactions, enzymes, and biochemical genetics. J. Amer. med. Ass. 165, 835–838 (1957).

    CAS  Google Scholar 

  • Motulsky, A. G.: Rapid detection of Glucose-6-phosphate dehydrogenyse deficiency in red cells. Distribution and frequency of the trait and its possible relationship to malaria. (Manuskr.).

    Google Scholar 

  • Mourant, A. E.: The distribution of the human blood groups. Oxford 1954.

    Google Scholar 

  • Mourant, A. E.: Anthropology and natural selection of blood groups. Acta genet. (Basel) 6, 509–515 (1957).

    CAS  Google Scholar 

  • Müller, M.: Die Häufigkeit der Blutsverwandtenehen der katholischen Bevölkerung der Gesamtdiözese Münster von 1944–1951 und des oldenburgischen Teiles der Diözese von 1899–1951. Diss. Münster 1953.

    Google Scholar 

  • Müller, H. J.: The problem of genie modification. Verh. 5. int. Kongr. Vererb. Wiss. Z. indukt. Abstamm.- u. Vererb.-Lehre Suppl. 1, 234–260 (1927).

    Google Scholar 

  • Müller, H. J.: Our load of mutations. Amer. J. hum. Genet. 2, 111–176 (1950) (a).

    Google Scholar 

  • Müller, H. J.: Radiation damage to the genetic material. Amer. Scientist 38, 33–60 (1950) (b).

    Google Scholar 

  • Müller, H. J.: Strahlenwirkung und Mutation beim Menschen. Naturwiss. Rdsch. 9, 127–135 (1956).

    Google Scholar 

  • Müller, H. J.: Further studies bearing on the load of mutations in man. Acta genet. (Basel) 6, 157–168 (1957).

    Google Scholar 

  • Müller, H. J. and L. M. Mott-Smith: Evidence that natural radioactivity is inadequate to explain the frequency of “natural” mutations. Proc. nat. Acad. Sci. (Wash.) 16 (1930).

    Google Scholar 

  • Murakami, U.: Clinico-genetic study of heredi tary disorders of the nervous system, especially on problems of phenogenesis. Folia psychiatr. Jap. Suppl. I (1957).

    Google Scholar 

  • Nachtsheim, H.: Die Mutationsrate menschlicher Gene. Naturwissenschaften 41, 385–392 (1954) (a).

    Google Scholar 

  • Nachtsheim, H.: Die Mutabilität menschlicher Gene. Caryologia 6, 139–154 (1954) (b).

    Google Scholar 

  • Nachtsheim, H.: Mutation und Phänokopie bei Säugetier und Mensch. Experientia (Basel) 13, 57–68 (1957).

    CAS  Google Scholar 

  • Nachtsheim, H.: Atomenergie und Erbgut. Münch, med. Wschr. 99, 1283–1290 (1957).

    CAS  Google Scholar 

  • Nachtsheim, H.: Die Bedeutung genetischer Faktoren für die Entstehung von Mißbildungen und Mißbildungskrankheiten. Verh. dtsch. Ges. inn. Med. 64, 33–50 (1958).

    Google Scholar 

  • Nakamura, H., M. Yoshiga, K. Kaziro and G. Kikuchi: On “anenzymia catalasea”, a new type of constitutional abnormality. Proc. Jap. Acad. 28, 59–64 (1952).

    CAS  Google Scholar 

  • Neel, J. V.: The study of human mutation rates. Amer. Naturalist 86, 129–144 (1952).

    Google Scholar 

  • Neel, J. V.: The genetics of human haemoglobin differences: problems and perspectives. Ann. hum. Genet. 21, 1–30 (1956).

    PubMed  CAS  Google Scholar 

  • Neel, J. V.: The detection of the genetic carriers of hereditary disease. Amer. J. hum. Genet. 1, 19–36 (1949).

    PubMed  CAS  Google Scholar 

  • Neel, J. V.: The detection of the genetic carriers of inherited disease. Clinical Genetics, Ed. A. Sorsby. London 1953.

    Google Scholar 

  • Neel, J. V.: Problems in the estimation of the frequency of uncommon inherited traits. Amer. J. hum. Genet. 6, 51–59 (1954).

    PubMed  CAS  Google Scholar 

  • Neel, J. V.: The genetics of human haemoglobin differences: problems and perspectives. Ann. hum. Genet. 21, 1–30 (1956).

    PubMed  CAS  Google Scholar 

  • Neel, J. V., W. J. Schull, D. J. McDonald, N. E. Morton, M. Kodani, K. Takeshima, R. C. Anderson, J. Wood, R. Brewer, S. Wright, J. Yamazaki, M. Suzuki and S. Kitamura: The effect of exposure to the atomic bombs on pregnancy termination in Hiroshima and Nagasaki. Nat. Res. Counc. Publ. 1956, 461.

    Google Scholar 

  • Neel, J. V.: Some problems in the estimation of spontaneous mutation rates in animals and man. Effects of radiation on human heredity, Wld Hlth Organization, Geneva 1957 a.

    Google Scholar 

  • Neel, J. V.: Some problems inherent in the study of human genetics with particular reference to the evaluation of radiation risks. Proc. nat. Acad. Sei. (Wash.) 43, 736–744 (1957b).

    Google Scholar 

  • Neel, J. V.: The study of natural selection in primitive and civilized human populations. Human Biol. 30, 43–72 (1958).

    PubMed  CAS  Google Scholar 

  • Oehlkers, F.: Die Auslösung von Chromosomenmutationen in der Meiosis durch Einwirkung von Chemikalien. Z. indukt. Abstamm.- u. Vererb.-Lehre 81, 313–341 (1943).

    Google Scholar 

  • Orel, H.: Die Verwandtenehen in der Erzdiözese Wien. Arch. Rassenbiol. 26, 249 — 278 (1932).

    Google Scholar 

  • Ott, H.: Das Blutserum bei Analbuminämie. Weitere Untersuchungen über die Serumfraktionen, das Farbstoffbindungsvermögen und den kolloid-osmotischen Druck. Z. ges. exp. Med. 128, 340–360 (1957).

    PubMed  CAS  Google Scholar 

  • Patau, H., u. H. Nachtsheim: Mutationsdruck und Selektionsdruck beim Pelger-Gen des Menschen. Z. Naturforsch. 1, 345–348 (1946).

    Google Scholar 

  • Patterson, R. M., B. K. Bagchi and A. Test: The prediction of Huntington’s chorea. An electroencephalographic and genetic study. Amer. J. Psychiat. 104, 786 (1948).

    PubMed  CAS  Google Scholar 

  • Pauling, L., H. A. Itano, S. J. Singer and I. C. Wells: Sickle cell anemia, a molecular disease. Science 110, 543–548 (1949).

    PubMed  CAS  Google Scholar 

  • Penrose, L. S.: The problem of anticipation in pedigress of dystrophia myotonica. Ann. Eugen. (Lond.) 14, 125–132 (1947–49).

    Google Scholar 

  • Penrose, L. S.: The supposed threat of declining intelligence. Amer. J. ment. Defic. 53, 114–118 (1948).

    PubMed  CAS  Google Scholar 

  • Penrose, L. S.: Measurement of pleiotropic effects in phenylketonuria. Ann. Eugen. (Lond.) 16, 134–141 (1951–52).

    Google Scholar 

  • Penrose, L. S.: The general purpose sib-pair linkage test. Ann. Eugen. (Lond.) 18, 120–124 (1953–54).

    Google Scholar 

  • Penrose, L. S.: Some recent trends in human genetics. Atti del IX. Int. Congr. Genet. Bellagio, 1953. Caryologia Suppl., 521–530 (1954).

    Google Scholar 

  • Penrose, L. S.: Parental age and mutation. Lancet 1955 II, 312.

    Google Scholar 

  • Penrose, L. S.: In: Die Strahlengefährdung des Menschen. Bericht des medizinischen Forschungsrates in Großbritannien (Dtsch. Übers.). Bonn 1956 (a).

    Google Scholar 

  • Penrose, L. S.: Mutation in man. Acta genet. (Basel) 6, 169–182 (1956) (b).

    Google Scholar 

  • Penrose, L. S.: Parental age in achondroplasia and mongolism. Amer. J. hum. Genet. 9, 167–169 (1957).

    PubMed  CAS  Google Scholar 

  • Penrose, L. S., S. M. Smith and D. A. Sprott: On the stability of allelic systems, with special reference to haemoglobins A, S and C. Ann. hum. Genet. 21, 90–93 (1956–57).

    Google Scholar 

  • Penrose, L. S.: A note on the prevalence of genes for deleterious recessive traits in man. Ann. hum. Genet. 21, 222–223 (1957).

    PubMed  CAS  Google Scholar 

  • Penrose, L. S. and C. Stern: Reconsideration of the Lambert pedigree (ichthyosis hystrix gravior). Ann. hum. Genet. 22, 258–283 (1958).

    PubMed  CAS  Google Scholar 

  • Pfändler, U.: La manifestation hétérozygote et homozygote de certains troubles du métabolisme (porphyrie chronique, cystinose, maladie de Niemann-Pick). Acta genet. (Basel) 7, 184–187 (1957).

    Google Scholar 

  • Pfändler, U.: L’ importance des facteurs génétiques dans les troubles métaboliques de l’enfant. Mod. Probl. Paediat. 3, 542–592 (1957).

    Google Scholar 

  • Pfändler, U.: La contribution de la biochimie au développement de la phénogénétique humaine. Rev. int. Vitaminol. 28, 110–118 (1957).

    Google Scholar 

  • Pontecorvo, G., et al.: The genetics of aspergillus nidulans. Advanc. Genetics 5, 141–238 (1953).

    CAS  Google Scholar 

  • Prokop, O.: Blutgruppen und Krankheit. Dtsch. med. Wschr. 1958, 431–433.

    Google Scholar 

  • Race, R. R., and R. Sanger: Blood groups in man. 3. Aufl. Oxford: Blackwell Scientific Publications 1958.

    Google Scholar 

  • Raper, A. B.: Sickling and malaria. Brit. med. J. 1954 II, 1163.

    Google Scholar 

  • Raper, A. B.: Malaria and the sickling trait. Brit. med. J. 1955, 1186–1189.

    Google Scholar 

  • Rayner, S.: Juvenile amaurotic idioty. Diagnosis of heterozygotes. Acta genet. (Basel) 3, 1–5 (1952).

    CAS  Google Scholar 

  • Reed, S. C.: A test for heterozygous deleterious recessives. J. Hered. 45, 17–18 (1954).

    Google Scholar 

  • Reed, T. E.: Tests of models representing selection in mother-child data on ABO blood groups Amer. J. hum. Genet. 8, 257–268 (1956).

    CAS  Google Scholar 

  • Reed, T. E.: The definition of relative fitness of individuals with specific genetic traits. Amer. J. hum. Genet, (im Druck).

    Google Scholar 

  • Reed, T. E.: and H. F. Falls: A pedigree of aniridia with a discussion of germinal mosaicism in man. Amer. J. hum. Genet. 7, 28–38 (1955).

    PubMed  CAS  Google Scholar 

  • Reed, T. E.: and J. V. Neel: A genetic study of multiple polyposis of the colon (with an appendix deriving a method of estimating relative fitness). Amer. J. hum. Genet. 7, 236–263 (1955).

    PubMed  CAS  Google Scholar 

  • Reed, T. E.: and J. V. Neel: Huntington’s chorea in Michigan. Amer. J. hum. Genet, (im Druck).

    Google Scholar 

  • Renwick, J. H.: Nail-patella syndrome: evidence for modification by alleles at the main locus. Ann. hum. Genet. 21, 159–169 (1956–57).

    Google Scholar 

  • Reed, T. E. and S. D. Lawler: Genetical linkage between the ABO and nail-patella loci. Ann. hum. Genet. 19, 312–331 (1955).

    Google Scholar 

  • Rosin, S., J. K. Moor-Jankowski u. M. Schneeberger: Die Fertilität im Bluterstamm von Tenna (Hämophilie B). Acta genet. (Basel) 8, 1–24 (1958).

    CAS  Google Scholar 

  • Rüdin, E.: Vorläufiger Bericht über den Gesundheitszustand von Kindern aus nahen Blutsverwandtenehen. Acta genet. (Basel) 7, 55–58 (1957).

    Google Scholar 

  • Rukavina, J. G., W. D. Block and A. C. Curtis: Familial primary systemic amyloidosis. An experimental, genetic and clinical study. J. invest. Derm. 27, 111–131 (1956) (a).

    Google Scholar 

  • Rukavina, J. G., W. D. Block and A. C. Curtis: Ultracentrifugal analysis of serum lipoproteins in familial primary systemic amyloidosis. J. Lab. clin. Med. 47, 365–369 (1956) (b).

    Google Scholar 

  • Sachs, L.: Sex-linkage and the sex chromosome in man. Ann. hum. Genet. 18, 255–261 (1953–54).

    Google Scholar 

  • Sanger, F.: In Currents in biochemical research (Ed. D. E. Green ). New York: Interscience Publ. 1956.

    Google Scholar 

  • Di Sant’ Agnese, P. A.: Fibrocystic disease of pancreas with normal or partial pancreatic function. Pediatrics 15, 683–697 (1955).

    Google Scholar 

  • Sartori, E.: Elementi per una teoria genetica del favismo. Acta paediat. lat. 10, 505–517 (1957).

    Google Scholar 

  • Sawin, P. B., and D. Glick: Atropinesterase, a genetically determined enzyme in the rabbit. Proc. nat. Acad. Sci. (Wash.) 29, 55–59 (1943).

    CAS  Google Scholar 

  • Schull, W. J.: Empirical risks in consanguineous marriages: Sex ratio, malformation, and viability. Amer. J. hum. Genet. 10, 294–343 (1958).

    PubMed  CAS  Google Scholar 

  • Schull, W. J. and J. V. Neel: Radiation and the sex ratio in man. Science 128, 343–348 (1958).

    PubMed  CAS  Google Scholar 

  • Schulze, Ch.: Erbbedingte Strukturanomalien menschlicher Zähne. München u. Berlin: Urban & Schwarzenberg 1956.

    Google Scholar 

  • Schulze, Chr., u. F. Lenz: Über Zahnschmelzhypoplasie von unvollständig dominantem geschlechtsgebundenem Erbgang. Z. menschl. Vererb.- u. Konstit.-Lehre. 31, 104–114 (1952).

    CAS  Google Scholar 

  • Schwarz u. Mitarbeiter(1956), zitiert nach Kalckar (1957).

    Google Scholar 

  • Seedorf, K. S.: Osteogenesis imperfecta. Kopenhagen 1951.

    Google Scholar 

  • Sekino, Y., I. Imamura and T. Yamaguchi: Psychiat. neurol. Jap. 58, 188 (1956).

    Google Scholar 

  • Siemens, H. W.: Über einen, in der menschlichen Pathologie noch nicht beobachteten Vererbungsmodus: Dominant-geschlechtsgebundene Vererbung. Arch. Rassenbiol. 17, 47–61 (1925).

    Google Scholar 

  • Singer, K., B. Fisher and M. A. Perlstein: Acanthrocytosis; a genetic erythrocytic malformation. Blood 7, 577–591 (1952).

    PubMed  CAS  Google Scholar 

  • Silvestroni, E., I. Bianco, G. Montalenti and M. Siniscalco: Genetic equilibrium of microcythaemia in some Italian districts. Nature (Lond.) 173, 357 (1954).

    CAS  Google Scholar 

  • Siniscalco, M.: Fitness of microcythaemics: a correction. Nature (Lond.) 176, 84–85 (1955).

    Google Scholar 

  • Sjögren, T., and T. Larsson: Microphthalmus and anophthalmus with or without coincident oligophrenia. A clinical and genetic-statistical study. Acta psychiat. scand. Suppl. 56 (1949).

    Google Scholar 

  • Slatis, H. M.: Comments on the rate of mutation to chondrodystrophy in man. Amer. J. hum. Genet. 7, 76 (1955).

    PubMed  CAS  Google Scholar 

  • Slatis, H. M.: A method of estimating the frequency of abnormal autosomal recessive genes in man. Amer. J. hum. Genet. 6, 412–418 (1954).

    PubMed  CAS  Google Scholar 

  • Slatis, H. M., R. H. Reis and R. E. Hoene: Consanguineous marriages in the Chicago region. Amer. J. hum. Gemet. 10, 446–464 (1958).

    CAS  Google Scholar 

  • Smith, A. J., and L. B. Strang: An inborn error of metabolism with urinary excretion of hydroxy-butyric acid and phenylpyruvic acid. Arch. Dis. Childh. 33, 109 (1958).

    PubMed  CAS  Google Scholar 

  • Smith, C. A. B.: The detection of linkage in human genetics. J. roy. Statist. Soc. 15, 153–192 (1953).

    Google Scholar 

  • Smith, C. A. B.: Counting methods in genetical statistics. Ann. hum. Genet. 21, 254–276 (1956–57).

    Google Scholar 

  • Smith, C. A. B.: A test for segregation ratios in family data. Ann. hum. Genet. 20, 257–265 (1955–56).

    Google Scholar 

  • Smith, C. A. B. and S. J. Kilkpatrick: Estimates od the sex ratio of mutation rates in sex-linked conditions by the method of maximum likelihood. Ann. hum. Genet. 22, 244–249 (1958).

    PubMed  CAS  Google Scholar 

  • Smith, S. M.: Notes on sickle-cell polymorphism. Ann. hum. Genet. 19, 51–57 (1954).

    PubMed  CAS  Google Scholar 

  • Smithies, O.: Grouped variations in the occurrence of new protein components in normal human serum. Nature (Lond.) 175, 307–308 (1955) (a).

    Google Scholar 

  • Smithies, O.: Zone electrophoresis in starch gels: Group variations in the serum proteins of normal human adults. Biochem. J. 61, 629–641 (1955) (b).

    Google Scholar 

  • Smithies, O.: Variations in human serum ß-globulins. Nature (Lond.) 180, 1482–1483 (1957).

    CAS  Google Scholar 

  • Smithies, O.: Third allele of the serum ß-globulin locus in humans. Nature (Lond.) 181, 1203–1204 (1958).

    CAS  Google Scholar 

  • Smithies, O., and N. F. Walker: Genetic control of some serum proteins in normal humans. Nature (Lond.) 176, 1265–1266 (1955).

    CAS  Google Scholar 

  • Smithies, O., and N. F. Walker: Notation for serum-protein groups and the genes controlling their inheritance. Nature (Lond.) 178, 694–695 (1956).

    CAS  Google Scholar 

  • Snyder, L. H.: Studies in human inheritance. X. A table to determine the proportion of recessives to be expected in various matings involving a unit character. Genetics 19, 1–17 (1934).

    PubMed  CAS  Google Scholar 

  • Sobel, E. H., L. C. Clark, R. P. Fox and M. Robinow: Rickets, deficiency of “alkaline” phosphatase activity and premature loss of teeth in childhood. Pediatrics 11, 309–322 (1953).

    PubMed  CAS  Google Scholar 

  • Sonneborn, T. M.: Paternal age and stillbirth in man. Ree. Gen. Soc. Amer. 25, 661 (1956).

    Google Scholar 

  • Sonneborn, T. M.: Early human death rate in relation to paternal age. Ree. Gen. Soc. Amer. 26, 397 (1957).

    Google Scholar 

  • Speiser, P.: Bestehen mathematisch gesicherte Beziehungen der ABO-Gruppen, des Rhesusfaktors Rh0 (D) und des Geschlechtes zu Carcinoma ventriculi, Ulcus ventriculi und Ulcus duodeni ? Krebsarzt 6, 344–348 (1956).

    Google Scholar 

  • Spiegelman, S. and R. Dunn: Interactions between enzyme-forming systems during adaption. J. gen. Physiol. 31, 153–173 (1947).

    PubMed  CAS  Google Scholar 

  • Spuhler, J. N.: Estimation of mutation rates in man. Clin. Orthopaed. 8, 34–43 (1956).

    CAS  Google Scholar 

  • Stadler, L. J.: Genetic effects of X-rays in maize. Proc. nat. Acad. Sci. (Wash.) 14, 60–75 (1928).

    Google Scholar 

  • Stephens, F. E., and F. H. Tyler: Studies in disorders of muscle. V. The inheritance of childhood progressive muscular dystrophy in 33 kindreds. Amer. J. hum. Genet. 3, 111–125 (1951).

    CAS  Google Scholar 

  • Stephens, F. E., G. T. Perkoff, D.-A. Dolowitz and F. H. Tyler: Partially sex-linked dominant inheritance of interstitial pyelonephritis. Amer. J. hum. Genet. 3, 303–313 (1951).

    PubMed  CAS  Google Scholar 

  • Stern, C.: The problem of complete Y-linkage in man. Amer. J. hum. Genet. 9, 147–165 (1957).

    PubMed  CAS  Google Scholar 

  • Stern, C.: Principles of human genetics. Deutsche Ausgabe: Grundlagen der menschlichen Erblehre. Übers, v. E. Wolf. Göttingen 1955.

    Google Scholar 

  • Stevenson, A. C.: Muscular dystrophy in Northern Ireland. II. An account of nine additional families. Ann. hum. Genet. 19, 159–164 (1955).

    PubMed  CAS  Google Scholar 

  • Stevenson, A. C.: In: Strahlenwirkung auf menschliche Erbanlagen. Strahlenschutz 3 (1957).

    Google Scholar 

  • Stevenson, A. C.: Muscular dystrophy in Northern Ireland. I. An account of the condition in fifty-one families. Ann. Eugen. (Lond.) 18, 50–93 (1953).

    CAS  Google Scholar 

  • Stevenson, A. C., E. A. Cheeseman and M. C. Huth: Muscular dystrophy in Northern Ireland. III. Linkage data with particular reference to autosomal limb girdle muscular dystrophy. Ann. hum. Genet. 19, 165–173 (1955).

    PubMed  CAS  Google Scholar 

  • Strobel, D., u. F. Vogel: Ein statistischer Gesichtspunkt für das Planen von Untersuchungen über Änderungen der Mutationsrate beim Menschen. Acta gent. (Basel) 8, 274–286 (1958).

    Google Scholar 

  • Struthers, D.: ABO groups of infants and children dying in the West of Scotland (1949–1951). Brit. J. Social Med. 5, 223–228 (1951).

    CAS  Google Scholar 

  • Sutton, H. E.: The distribution of haptoglobin types and their genetic implications. Proc. X. int. Congr. Genet. 1958 II, 284.

    Google Scholar 

  • Sutton, H. E., J. V. Neel, G. Binson and W. W. Zuelzer: Serum protein differences between Africans and Caucasians. Nature (Lond.) 178, 1287 (1956).

    CAS  Google Scholar 

  • Sutton, H. E., J. V. Neel, F. B. Livingstone, G. Binson, P. Kunstadter and L. E. Trombley: The frequencies of haptoglobin types in five populations. Ann. hum. Genet, (im Druck).

    Google Scholar 

  • Sutton, H. E. and J. H. Read: Abnormal amino acid metabolism in a case suggesting autism. Amer. J. Dis. Child. 96, 23–28 (1958).

    Google Scholar 

  • Szeinberg, A., Y. Asher and C. Sheba: Studies on glutathione stability in erythrocytes of cases with past history of favism or sulfa-drug-induced hemolysis. Blood 13, 348–358 (1958)

    PubMed  CAS  Google Scholar 

  • Takahara, S.: Progressive oral gangrene probably due to lack of catalase in the blood (akatalasaemia) report of nine cases. Lancet 1952 II, 1101–1104.

    Google Scholar 

  • Tashian, R. E.: The role of enzyme adaptation in the heritability of variation in d-phenylalanine utilization in man. Proc. X. int. Congr. Genet. 1958 II, 289.

    Google Scholar 

  • Timoféeff-Ressovsky, N. W., u. K. G. Zimmer: Das Trefferprinzip in der Biologie. Leipzig 1947.

    Google Scholar 

  • Tjio, H. J., and A. Levan: The chromosome numbers of man. Hereditas (Lund) 42, 1–6 (1956) (a).

    Google Scholar 

  • Tjio, H. J., and A. Levan: Comparative idiogram analysis of the rat and Yoshida rat sarcoma. Hereditas (Lund) 42, 218–234 (1956) (b).

    Google Scholar 

  • Turunen, M., and M. Pasila: The ABO blood groups and carcinoma of the stomach. Ann. Med. exp. Fenn. 35, 100 (1957).

    PubMed  CAS  Google Scholar 

  • Vandepitte, J. M., W. W. Zuelzer, J. V. Neel and J. Colaert: Evidence concerning the inadequacy of mutation as an explanation of the frequency of the sickle-cell gene in the Belgian Kongo. Blood 10, 341–350 (1955).

    PubMed  CAS  Google Scholar 

  • Verschtter, O. v.: Wirksame Faktoren im Leben des Menschen. Wiesbaden: F. Steiner 1954.

    Google Scholar 

  • Verschtter, O. v.: Tuberkulose und Krebs bei Zwillingen. Acta genet. (Basel) 6, 103–113 (1956).

    Google Scholar 

  • Verschtter, O. v.: Über den methodischen Beitrag der Zwillingsforschung für die Humangenetik. Acta genet. (Basel) 7, 21–32 (1957).

    Google Scholar 

  • Verschtter, O. v.: Die Zwillingsforschung im Dienste der inneren Medizin. Verh. dtsch. Ges. inn. Med. 64, 262–273 (1958).

    Google Scholar 

  • Vogel, F.: The mutation rate of the Rh-loci — a critical review. Amer. J. hum. Genet. 6, 279–283 (1954).

    PubMed  CAS  Google Scholar 

  • Vogel, F.: Über Genetik und Mutationsrate des Retinoblastoms. Z. menschl. Vererb.- u. Konstit.- Lehre 82, 308–336 (1954).

    Google Scholar 

  • Vogel, F.: Über eine Modifikation der Dahlbergschen Methode zur Schätzung menschlicher Mutationsraten. Acta genet. (Basel) 5, 63–71 (1954).

    CAS  Google Scholar 

  • Vogel, F.: Vergleichende Betrachtungen über die Mutationsrate der geschlechtsgebunden-rezessiven Hämophilieformen in der Schweiz und in Dänemark. Blut 1, 91–109 (1955) (a).

    Google Scholar 

  • Vogel, F.: Neue Ergebnisse der Hämophilie-Forschung. Blut 1, 214–222 (1955) (b).

    Google Scholar 

  • Vogel, F.: Über die Prüfung von Modellvorstellungen zur spontanen Mutabilität an menschlichem Material. Z. menschl. Vererb.- u. Konstit.-Lehre 33, 470–491 (1956).

    CAS  Google Scholar 

  • Vogel, F.: Neue Untersuchungen zur Genetik des Retinoblastoms (Glioma retinae). Z. menschl. Vererb.- u. Konstit.-Lehre 34, 205–236 (1957) (a).

    Google Scholar 

  • Vogel, F.: Die eugenische Beratung beim Retinoblastom (Glioma retinae). Acta genet. (Basel) 7, 565–572 (1957) (b).

    Google Scholar 

  • Vogel, F.: Elektroencephalographische Untersuchungen an gesunden Zwillingen. Acta genet. (Basel) 7, 334–337 (1957) (c).

    Google Scholar 

  • Vogel, F.: Gedanken über den Mechanismus einiger spontaner Mutationen beim Menschen. Z. menschl. Vererb.- u. Konstit.-Lehre 34, 389–399 (1958) (a).

    Google Scholar 

  • Vogel, F.: Verzögerte Mutation beim Menschen? Einige kritische Bemerkungen zu CHarlotte AIterbachs Arbeit. Ann. hum. Genet. 22, 132–137 (1958) (b).

    Google Scholar 

  • Vogel, F.: Über die Erblichkeit des normalen Elektroencephalogramms. Vergleichende Untersuchungen an ein- und zweieiigen Zwillingen. Stuttgart: Georg Thieme 1958 (c).

    Google Scholar 

  • Vogel, F.: Zur Problematik induzierter Mutationen beim Menschen. Röntgenblätter 9, 193–205 1958, (d).

    Google Scholar 

  • Vogel, F.: Die erblichen Blutkrankheiten und ihre anthropologische Bedeutung. Verh. dtsch. Anthrop.

    Google Scholar 

  • Vogel, F.: Ges. 1958 (e).

    Google Scholar 

  • Vogel, F.: u. W. Götze: Familienuntersuchungen zur Genetik des normalen Elektroencephalogramms. Dtsch. Z. Nervenheilk. 178, 668–700 (1959).

    Google Scholar 

  • Waardenburg, P. J.: Zum Kapitel des außerokularen erblichen Nystagmus. Acta gent. (Basel) 4, 298–312 (1953).

    CAS  Google Scholar 

  • Wagner, R. P., and H. K. Mitchell: Genetics and metabolism. New York-London 1955.

    Google Scholar 

  • Walton, J. N.: On the inheritance of muscular dystrophy. Ann. hum. Genet. 20, 1–38 (1955).

    PubMed  CAS  Google Scholar 

  • Walton, J. N.: On the inheritance of muscular dystrophy. Ann. hum. Genet. 20, 1–38 (1955). Watson, J. D., and F. H. C. Crick: The structure of DNA. Cold Spr. Harb. Symp. quant. Biol. 18, 123–132 (1953).

    Google Scholar 

  • Wendt, G. G.: Die Verantwortung der Ärzteschaft bei der Anwendung von Röntgenstrahlen und anderen ionisierenden Strahlen. Dtsch. med. Wschr. 82, 392–393 (1957d).

    Google Scholar 

  • Walton, J. N.: Der Fortschritt der ärztlichen Kunst als Gefahr für die biologische Zukunft der Menschheit. Dtsch. med. Wschr. 82, 1676–1681 (1957b).

    Google Scholar 

  • Walton, J. N. u. B. E. Wolf: Die Chromosomenzahl beim Menschen. Dtsch. med. Wschr. 1957, 1832–1836.

    Google Scholar 

  • Williams, R. J.: Biochemical individuality. New York: John Wiley & Sons 1956.

    Google Scholar 

  • Winters, R. W., J. B. Graham, T. F. Williams, V. W. McFalls and C. H. Burnett: A genetic study of familial hypophosphatemia and vitamin D-resistant rickets. Trans. Ass. Amer. Physicians 70, 234–242 (1957).

    PubMed  CAS  Google Scholar 

  • Woolf, B.: On estimating the relation between blood groups and disease. Ann. hum. Genet. 19, 251–253 (1955).

    PubMed  CAS  Google Scholar 

  • Walton, J. N., R. Griffith and A. Moncrieff: Treatment of phenylketonuria with a diet low in Phenylalanin. Brit. med. J. 1955 I, 57–64.

    Google Scholar 

  • Woolley, D. W.: Manipulation of cerebral serotonin and its relationship to mental disorders. Science 125, 752 (1957).

    Google Scholar 

  • Wuhrmann, F., u. Ch. Wunderly: Die Bluteiweißkörper des Menschen. 3. Aufl. Basel: B. Schwabe 1957.

    Google Scholar 

  • Zuelzer, W. W., J. V. Neel and A. R. Robinson: Abnormal hemoglobins. Progress in Hematology. p. 91–137. Grune & Stratton 1956.

    Google Scholar 

  • Zup**er, A.: Biologische Strahlengefährdung. Ergebn. inn. Med. Kinderheilk. N. F. 10, 362–382 (1958).

    CAS  Google Scholar 

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  1. Max Planck-Institut für vergleichende Erbbiologie und Erbpathologie, Berlin-Dahlem, Deutschland

    Friedrich Vogel

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  1. Friedrich Vogel
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  1. Freiburg i. Br., Deutschland

    L. Heilmeyer

  2. Göttingen, Deutschland

    R. Schoen

  3. Frankfurt a. M., Deutschland

    B. de Rudder

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Vogel, F. (1959). Moderne Probleme der Humangenetik. In: Heilmeyer, L., Schoen, R., de Rudder, B. (eds) Ergebnisse der Inneren Medizin und Kinderheilkunde. Ergebnisse der Inneren Medizin und Kinderheilkunde, vol 12. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-94744-5_2

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