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Human Heredity|April 3, 2009
Multiple imputation to correct for measurement error in admixture estimates in genetic structured association testingMiguel A Padilla, Jasmin Divers, Laura K Vaughan, et al.Human Heredity|January 1, 1991
Hereditary disorders in Saguenay-Lac-St-Jean (Quebec, Canada)M De BraekeleerHuman Heredity|January 1, 1991
Impact of heredity in myopiaJ M Teikari, J O'Donnell, J Kaprio, et al.Human Heredity|January 1, 1991
Population studies in northern Sweden. XVII. Estimates of Finnish and Saamish influenceP O Nylander, L BeckmanHuman Heredity|January 1, 1991
Founder effect in familial hyperchylomicronemia among French Canadians of QuebecM De Braekeleer, C Dionne, C Gagné, et al.Human Heredity|January 1, 1991
Polymorphism of complement component I in Mongoloid populations: a new genetic variant IF A2M Ding, K Umetsu, I Yuasa, et al.Human Heredity|January 1, 1989
Genetic genealogical studies of 20 north Swedish families with the rare blood group pS Nordström, B CedergrenHuman Heredity|January 1, 1989
High frequency of the rapid isoniazid acetylator phenotype in Lagos (Nigeria)P G Odeigah, M A OkunowoHuman Heredity|January 1, 1989
Plasma alpha 1B-glycoprotein allele frequencies in Finns and Swedish Lapps: evidence for a new alpha 1B alleleR K Juneja, G Beckman, M Lukka, et al.Human Heredity|January 1, 1989
Alpha 2 HS-glycoprotein phenotype and allele distribution in continental Italy and SardiniaR Scacchi, P Lucarelli, R M CorboPageof 237