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Human Genetics|December 1, 1986
Alpha-thalassemia in Papua New GuineaP Yenchitsomanus, K M Summers, P G Board, et al.Human Genetics|December 1, 1986
Choroideremia: further evidence for assignment of the locus to Xq13-Xq21M Schwartz, T Rosenberg, E Niebuhr, et al.Human Genetics|December 1, 1986
Origin of new mutations in Duchenne muscular dystrophyL Roncuzzi, A Ferlini, A Pirozzi, et al.Human Genetics|October 25, 2017
World-wide distributions of lactase persistence alleles and the complex effects of recombination and selectionAnke Liebert, Saioa López, Bryony Leigh Jones, et al.Human Genetics|October 1, 1988
A new RFLP with StuI and probe cX55.7 (DXS105) and its usefulness in carrier analysis of fragile X syndromeA M Rekilä, M L Väisänen, M Kähkönen, et al.Human Genetics|August 25, 2017
A multi-stage genome-wide association study of uterine fibroids in African AmericansJacklyn N Hellwege, Janina M Jeff, Lauren A Wise, et al.Human Genetics|January 1, 1988
A DNA polymorphism of an apoprotein gene associates with the hypertriglyceridaemia of primary goutG A Ferns, J Lanham, P Dieppe, et al.Human Genetics|January 1, 1988
Apolipoprotein gene cluster on chromosome 19. Definite localization of the APOC2 gene and the polymorphic Hpa I site associated with type III hyperlipoproteinemiaM Smit, E van der Kooij-Meijs, R R Frants, et al.Human Genetics|February 1, 1988
The use of DNA probes to establish parental origin in Down syndromeN L Rudd, L S Dimnik, C Greentree, et al.Human Genetics|September 1, 1987
Familial hypercholesterolemia in South African Afrikaners. PvuII and StuI DNA polymorphisms in the LDL-receptor gene consistent with a predominating founder gene effectP A Brink, L T Steyn, G A Coetzee, et al.Pageof 958