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Annals of Human Genetics|June 8, 2004
The Sib TDT adjusted for age of disease onsetSaurabh Ghosh, Theodore ReichAnnals of Human Genetics|October 8, 2004
Commingling analysis of intraocular pressure and glaucoma in an older Australian populationAnanth C Viswanathan, Roger A Hitchings, Andrea Indar, et al.Annals of Human Genetics|October 8, 2004
Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican familiesA Huertas-Vázquez, J P del Rincón, S Canizales-Quinteros, et al.Annals of Human Genetics|October 8, 2004
Compound haplotypes at Xp11.23 and human population growth in EurasiaS Alonso, J A L ArmourAnnals of Human Genetics|October 8, 2004
Genetic dissection of human stature in a large sample of multiplex pedigreesYao-Zhong Liu, Fu-Hua Xu, Hui Shen, et al.Annals of Human Genetics|October 8, 2004
Estimated frequency of genetic and nongenetic causes of congenital idiopathic cerebral palsy in west SwedenH CosteffAnnals of Human Genetics|July 1, 1993
Regional localization of the lactase-phlorizin hydrolase gene, LCT, to chromosome 2q21C B Harvey, M F Fox, P A Jeggo, et al.Annals of Human Genetics|July 1, 1993
Regional localization of the gene coding for the GM2 activator protein (GM2A) to chromosome 5q32-33 and confirmation of the assignment of GM2AP to chromosome 3D M Swallow, I Islam, M F Fox, et al.Annals of Human Genetics|November 4, 2005
The association of mitochondrial DNA 5178 C > a polymorphism with plasma lipid levels among three ethnic groupsS Lal, M Madhavan, C K HengAnnals of Human Genetics|November 4, 2005
Possible association of the human KCNE1 (minK) gene and QT interval in healthy subjects: evidence from association and linkage analyses in Israeli familiesY Friedlander, M Vatta, N Sotoodehnia, et al.Pageof 231