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Annals of Human Genetics|December 7, 2006
Osteoprotegerin plasma levels are strongly associated with polymorphisms in human homologue of the mouse progressive ankylosis (ANKH) geneY Vistoropsky, I Malkin, E Kobyliansky, et al.Annals of Human Genetics|November 14, 2006
Molecular epidemiology of phenylalanine hydroxylase deficiency in Southern Italy: a 96% detection rate with ten novel mutationsA Daniele, G Cardillo, C Pennino, et al.Annals of Human Genetics|December 15, 2006
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4A Tlili, S Masmoudi, H Dhouib, et al.Annals of Human Genetics|July 1, 1991
Kinship structures and migration in the Po DeltaI Barrai, R Canella, M Beretta, et al.Annals of Human Genetics|July 21, 2007
The impact of BRCA1 on spina bifida meningomyelocele lesionsTerri M King, Kit-Sing Au, Timothy J Kirkpatrick, et al.Annals of Human Genetics|May 18, 2007
Interleukin 6 variable number of tandem repeats (VNTR) gene polymorphism in centenariansC Capurso, V Solfrizzi, A D'Introno, et al.Annals of Human Genetics|May 31, 2007
Association of microsatellite polymorphisms of the human 14q13.2 region with type 2 diabetes mellitus in Latvian and Finnish populationsT Sjakste, M Kalis, I Poudziunas, et al.Annals of Human Genetics|June 9, 2007
Persistence of the common Hartnup disease D173N allele in populations of European originDimitar N Azmanov, Helen Rodgers, Christiane Auray-Blais, et al.Annals of Human Genetics|May 25, 2007
Sample size needed to detect gene-gene interactions using linkage analysisShuang Wang, Hongyu ZhaoAnnals of Human Genetics|May 25, 2007
Interaction of genetic risk factors confers higher risk for thrombotic stroke in male Chinese: a multicenter case-control studyChun-Duo Shen, Wei-Li Zhang, Kai Sun, et al.Pageof 231