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American Journal of Human Genetics|November 5, 1997
Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 geneP Manga, J G Kromberg, N F Box, et al.American Journal of Human Genetics|November 5, 1997
Mutation characterization and genotype-phenotype correlation in Barth syndromeJ Johnston, R I Kelley, A Feigenbaum, et al.American Journal of Human Genetics|November 5, 1997
The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative casesH C Tsou, D H Teng, X L Ping, et al.American Journal of Human Genetics|November 5, 1997
De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counselingB Wirth, T Schmidt, E Hahnen, et al.American Journal of Human Genetics|November 5, 1997
Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide searchP Gasparini, E Miraglia del Giudice, J Delaunay, et al.American Journal of Human Genetics|November 5, 1997
Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancerG R Bignell, F Canzian, M Shayeghi, et al.American Journal of Human Genetics|November 5, 1997
Evidence for locus heterogeneity in Puerto Ricans with Hermansky-Pudlak syndromeS Hazelwood, V Shotelersuk, S C Wildenberg, et al.American Journal of Human Genetics|November 5, 1997
Progressive ataxia due to a missense mutation in a calcium-channel geneQ Yue, J C Jen, S F Nelson, et al.American Journal of Human Genetics|November 1, 1977
Intrafamilial correlation analysis for IgM serum levelsJ Guízar-Vázquez, F P Saint-Martin, I Rostenberg, et al.American Journal of Human Genetics|November 1, 1977
Detection of genetic variation with radioactive ligands. I. Electrophoretic screening of plasma proteins with a selected panel of compoundsL L Cavalli-Sforza, S P Daiger, D P RummelPageof 979