51,309 Result(s)
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Tramvie elettriche
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Libri nuovi
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L'incandescenza a gas
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La fotosmaltografia
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Oidien und Oidiomykose
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Libri nuovi
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Über die Beziehungen des Vagus zum Sympathieus bei der Milz
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Search for optimum electric pulses to obtain tracks in isotropic monogap chambers
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Ultrastructural features of the muscle fibers in congenital hypothyroidism
Muscles of three patients (2 years, 2 years and 7 months, and 11 years of age) affected by congenital hypothyroidism due to dysgenesis of the thyroid gland were studied by electron microscope. The biopsies wer...
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Characterization of serum alkaline phosphatase in infancy and childhood
In 364 serum samples of cord blood, infants, children, and adults alkaline phosphatase was characterized by means of L-phenylalanine inhibition, L-homoarginine inhibition, heat inactivation, acrylamide gel dis...
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Multiple anomalies associated with an extra small metacentric chromosome: Modified Giemsa stain results
A female infant aged 10 months with multiple congenital anomalies associated with a small metacentric extra chromosome is reported. The chromosomal studies with a modified Giemsa-stain technique suggests that ...
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Transsexualism in Vietnam
The case described is that of a man raised in the Vietnamese peasant countryside who clearly fits the transsexual syndrome. On physical examination he appears to be a normal male, yet he insists that he is a f...
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A case of trisomy of the short arms of chromosome No. 4 with translocation t(4p 21p; 4q 21q) in the mother
The clinical features and cytogenetic Giemsa banding studies of a case of partial trisomy 4p [47,XX,+der(21), der(4), der(21), t(4p 21p;4q 21q) mat] are presented. This aberration resulted from a reciprocal tr...
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A case of extra small acrocentric bisatellited chromosome in a non mongoloid child
A mentally retarded child with an extra small bisatellited acrocentric chromosome is described. The patient exhibited rather unspecific clinical signs such as strabismus, marked facial asymmetry, broad and pro...
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A case of D13 ring chromosome
A case of D ring chromosome identified with trypsin banding as a 13 with loss of the bands p12 and q34 is reported. The clinical features characteristically associated with the loss of these specific segments ...
