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Nature Genetics|June 1, 1993
Direct detection of novel expanded trinucleotide repeats in the human genomeM Schalling, T J Hudson, K H Buetow, et al.Nature Genetics|March 1, 1993
Physical mapping of the holoprosencephaly critical region on chromosome 7q36F Gurrieri, B J Trask, G van den Engh, et al.Nature Genetics|April 1, 1996
Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiationM Burmeister, J Novak, M Y Liang, et al.Nature Genetics|April 1, 1996
Mouse Dax1 expression is consistent with a role in sex determination as well as in adrenal and hypothalamus functionA Swain, E Zanaria, A Hacker, et al.Nature Genetics|November 1, 1993
Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumoursE Friedman, P V Gejman, G A Martin, et al.Nature Genetics|November 1, 1993
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type IM Y Chung, L P Ranum, L A Duvick, et al.Nature Genetics|November 1, 1993
Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissuesT V Strong, D A Tagle, J M Valdes, et al.Nature Genetics|November 1, 1993
Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33T Toda, M Segawa, Y Nomura, et al.Nature Genetics|November 1, 1993
A homozygous insertion-deletion in the type VII collagen gene (COL7A1) in Hallopeau-Siemens dystrophic epidermolysis bullosaL Hilal, A Rochat, P Duquesnoy, et al.Pageof 744