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American Journal of Human Genetics|January 1, 1994
Three new mutations in patients with myophosphorylase deficiency (McArdle disease)S Tsujino, S Shanske, I Nonaka, et al.American Journal of Human Genetics|January 1, 1994
Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome IqJ E Richards, P R Lichter, M Boehnke, et al.American Journal of Human Genetics|January 1, 1994
Haplotype studies in Wilson diseaseG R Thomas, P C Bull, E A Roberts, et al.American Journal of Human Genetics|July 1, 1995
Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancerJ P Struewing, L C Brody, M R Erdos, et al.American Journal of Human Genetics|July 1, 1995
Genetic linkage heterogeneity in myotubular myopathyF Samson, L Mesnard, M Heimburger, et al.American Journal of Human Genetics|July 1, 1995
Tyrosinase inhibition due to interaction of homocyst(e)ine with copper: the mechanism for reversible hypopigmentation in homocystinuria due to cystathionine beta-synthase deficiencyO Reish, D Townsend, S A Berry, et al.American Journal of Human Genetics|July 1, 1995
Fine mapping of the congenital chloride diarrhea gene by linkage disequilibriumP Höglund, P Sistonen, R Norio, et al.American Journal of Human Genetics|January 1, 1981
Frequency of private electrophoretic variants and indirect estimates of mutation rate in Papua New GuineaK K Bhatia, N M Blake, S W Serjeantson, et al.American Journal of Human Genetics|January 1, 1981
Cardiac functioning and blood pressure of 47,XYY and 47,XXY men in a double-blind, double-matched population surveyE Boisen, D R Owen, L Rasmussen, et al.American Journal of Human Genetics|September 1, 1984
HLA-associated diseases: a new method for performing linkage analysis with other markers than HLAF Clerget-Darpoux, M C Babron, C Bonaïti-PelliePageof 979