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American Journal of Human Genetics|September 1, 1984
Parental HLA compatibility, fetal wastage and neural tube defects: evidence for a T/t-like locus in humansB Schacter, L R Weitkamp, W E Johnson
American Journal of Human Genetics|September 1, 1984
Beta-thalassemia in the Po Delta: selection, geography, and population structureI Barrai, A Rosito, G Cappellozza, et al.
American Journal of Human Genetics|September 1, 1984
The steroid sulfatase locus on structurally abnormal inactive X chromosomes is expressedL Immken, T Mohandas, R S Sparkes, et al.
American Journal of Human Genetics|January 1, 1984
Detection of genetic heterogeneity among pedigrees through complex segregation analysis: an application to hypercholesterolemiaP P Moll, T D Berry, W H Weidman, et al.
American Journal of Human Genetics|September 1, 1983
Duplication 9q34 syndromeP W Allderdice, B Eales, H Onyett, et al.
American Journal of Human Genetics|September 1, 1983
A new rare variant of the glyoxalase I system of the red cell: GLO-SicilyM Beretta, G Schilirò, A Russo, et al.
American Journal of Human Genetics|September 1, 1983
Intracellular folate distribution in cultured fibroblasts from patients with the fragile X syndromeB W Popovich, D S Rosenblatt, B A Cooper, et al.
American Journal of Human Genetics|August 1, 1995
Length heteroplasmy in the first hypervariable segment of the human mtDNA control regionK E Bendall, B C Sykes
American Journal of Human Genetics|August 1, 1995
A single amino acid substitution within the mature sequence of ornithine aminotransferase obstructs mitochondrial entry of the precursorT Kobayashi, H Ogawa, M Kasahara, et al.
American Journal of Human Genetics|August 1, 1995
A novel point mutation in a 3' splice site of the NADH-cytochrome b5 reductase gene results in immunologically undetectable enzyme and impaired NADH-dependent ascorbate regeneration in cultured fibroblasts of a patient with type II hereditary methemoglobinemiaK Shirabe, M T Landi, M Takeshita, et al.
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