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Human Heredity|November 26, 2002
Map error reduction: using genetic and sequence-based physical maps to order closely linked markersAndrew T DeWan, Antonio R Parrado, Tara C Matise, et al.Human Heredity|November 19, 2002
How do homozygous parents affect TDT as a test for association?Saurabh Ghosh, Theodore ReichHuman Heredity|July 30, 2002
Trend tests for case-control studies of genetic markers: power, sample size and robustnessB Freidlin, G Zheng, Z Li, et al.Human Heredity|January 1, 1975
Red cell glutamate-pyruvate transaminase gene frequencies in Gambia, West AfricaS G Welch, J Lee, I A McGregor, et al.Human Heredity|January 1, 1975
Validity of a screening test for typing serum cholinesterase variants among Greek populationsP K Das, C Kattamis, S Haidas, et al.Human Heredity|January 1, 1975
Suxamethonium sensitivity and segregation of human serum cholinesterase variants at locus, Ch1, among twelve British familiesP K DasHuman Heredity|January 1, 1975
A boy with 46, X, del, Y, due to a de nove mutationK Fried, M Rosenblatt, D VarsanoHuman Heredity|January 1, 1975
Haptoglobin type Hp-Jo and hypohaptoglobinaemia in a Danish family. Preliminary reportM Thymann, K HenningsenHuman Heredity|January 1, 1975
Parathenar palmar pattern: a dermatoglyphic sign of possible clinical significanceE B Hook, R BonenfantHuman Heredity|January 1, 1975
Incidence of congenital heart disease in HungaryM Mészáros, A Nagy, A CzeizelPageof 237