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American Journal of Human Genetics|December 1, 1993
Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA)R K Tripathi, S Bundey, M A Musarella, et al.
American Journal of Human Genetics|December 1, 1993
Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia AJ Oldenburg, R Schwaab, T Grimm, et al.
American Journal of Human Genetics|August 1, 1994
Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onsetL P Ranum, M Y Chung, S Banfi, et al.
American Journal of Human Genetics|August 1, 1994
Nature and recurrence of AVPR2 mutations in X-linked nephrogenic diabetes insipidusD G Bichet, M Birnbaumer, M Lonergan, et al.
American Journal of Human Genetics|August 1, 1994
Recurrent nonsense mutations within the type VII collagen gene in patients with severe recessive dystrophic epidermolysis bullosaA Hovnanian, L Hilal, C Blanchet-Bardon, et al.
American Journal of Human Genetics|August 1, 1994
Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cellsL Savelyeva, R Corvi, M Schwab
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