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American Journal of Human Genetics|July 1, 1997
XIST expression in human oocytes and preimplantation embryosR Daniels, M Zuccotti, T Kinis, et al.American Journal of Human Genetics|July 1, 1997
Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanningF Mirzayans, A J Mears, S W Guo, et al.American Journal of Human Genetics|July 1, 1997
Variable age at onset in insulin-dependent diabetes mellitus, by the marker-association-segregation-chi 2 methodN Bonneuil, A Clerget, F Clerget-DarpouxAmerican Journal of Human Genetics|December 17, 2005
A Y-chromosome signature of hegemony in Gaelic IrelandLaoise T Moore, Brian McEvoy, Eleanor Cape, et al.American Journal of Human Genetics|November 3, 2009
Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)nNozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, et al.American Journal of Human Genetics|February 1, 1991
Why are autism and the fragile-X syndrome associated? Conceptual and methodological issuesI L Cohen, V Sudhalter, A Pfadt, et al.American Journal of Human Genetics|February 1, 1991
High-resolution linkage mapping for susceptibility genes in human polygenic disease: insulin-dependent diabetes mellitus and chromosome 11qR N Hyer, C Julier, J D Buckley, et al.American Journal of Human Genetics|February 1, 1991
A mutation in the pro alpha 2(I) gene (COL1A2) for type I procollagen in Ehlers-Danlos syndrome type VII: evidence suggesting that skipping of exon 6 in RNA splicing may be a common cause of the phenotypeN S Vasan, H Kuivaniemi, B E Vogel, et al.American Journal of Human Genetics|October 1, 1992
A double mutation in exon 6 of the beta-hexosaminidase alpha subunit in a patient with the B1 variant of Tay-Sachs diseaseP J Ainsworth, M B Coulter-MackieAmerican Journal of Human Genetics|October 1, 1992
Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesteraseC P Nogueira, C F Bartels, M C McGuire, et al.Pageof 980