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  1. No Access

    Article

    The structure of DXF34, a human X-linked sequence family with homology to a transcribed mouse Y-linked repeat

    S. H. Laval, V. Reed, H. J. Blair, Y. Boyd in Mammalian Genome (1997)

  2. No Access

    Article

    Smcx lies distal to DXHX674 and DXHX679 on the mouse X Chromosome

    S. H. Laval, H. J. Blair, M. J. Mitchell, Y. Boyd in Mammalian Genome (1996)

  3. No Access

    Article

    The use of compound heterozygotes and Hprt selection to analyze X-linked mottled alleles associated with prenatal lethality

    X-linked mutant alleles associated with prenatal male lethality are difficult to analyze because only heterozygous females are readily available for study. Genomic analysis of the mutant allele is facilitated ...

    W. Masson, S. Holt, V. Reed, Y. Boyd in Mammalian Genome (1996)

  4. No Access

    Article

    Characterization and map** of the mouse NDP (Norrie disease) locus (Ndp)

    Norrie disease is a severe X-linked recessive neurological disorder characterized by congenital blindness with progressive loss of hearing. Over half of Norrie patients also manifest different degrees of menta...

    E. M. Battinelli, Y. Boyd, I. W. Craig, X. O. Breakefield, Z. -Y. Chen in Mammalian Genome (1996)

  5. No Access

    Article

    A somatic cell hybrid panel for mouse gene map** characterized by PCR and FISH

    P. Williamson, S. Holt, S. Townsend, Y. Boyd in Mammalian Genome (1995)

  6. No Access

    Article

    Evaluation of human microdissection clones from the FRAXA region as tools for comparative map** in the mouse: isolation of a conserved genomic clone close to FMR1

    H. J. Blair, M. C. Hirst, R. MacKinnon, K. E. Davies, Y. Boyd in Mammalian Genome (1994)

  7. No Access

    Article

    Map** of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse

    V. Reed, S. H. Laval, V. McCabe, H. F. Willard, Y. Boyd in Mammalian Genome (1994)

  8. No Access

    Article

    Map** of the agammaglobulinemia tyrosine kinase gene on the mouse X Chromosome with interspecific crosses

    R. W. Hendriks, V. Reed, Y. Boyd in Mammalian Genome (1994)

  9. No Access

    Article

    Map** of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin gene

    There are rare female patients who suffer from Duchenne or Becker muscular dystrophy because they carry an X;autosome translocation with a breakpoint in the dystrophin gene. We have defined the positions of se...

    D. J. Cockburn, E. A. Munro, I. W. Craig, Y. Boyd in Human Genetics (1992)

  10. No Access

    Article

    Gene deletions in patients with haemophilia B and anti-factor IX antibodies

    Christmas disease, or haemophilia B, is an inherited X-linked haemorrhagic disease which at present occurs in 798 known cases in the United Kingdom, corresponding to a frequency of about 1 in 30,000 males. Pat...

    F. Giannelli, K. H. Choo, D. J. G. Rees, Y. Boyd, C. R. Rizza, G. G. Brownlee in Nature (1983)