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Annals of Human Genetics|December 13, 2006
A novel genetic study of Chinese families with autosomal recessive retinitis pigmentosaM M Abd El-Aziz, M F El-Ashry, W M Chan, et al.Annals of Human Genetics|June 29, 2007
Mitochondrial and Y chromosome diversity in the English-speaking CaribbeanJ Benn Torres, R A Kittles, A C StoneAnnals of Human Genetics|June 16, 2009
Identifying putative promoter regions of Hermansky-Pudlak syndrome genes by means of phylogenetic footprintingHoria Stanescu, Tyra G Wolfsberg, R Travis Moreland, et al.Annals of Human Genetics|June 16, 2009
Association between SNP heterozygosity and quantitative traits in the Framingham Heart StudyDidahally R Govindaraju, Martin G Larson, Xiaoyan Yin, et al.Annals of Human Genetics|May 1, 1991
Family data determine all parameters in Mendelian incomplete penetrance modelsA S Whittemore, J B Keller, M J WardAnnals of Human Genetics|September 9, 2009
A variable-sized sliding-window approach for genetic association studies via principal component analysisRui Tang, Tao Feng, Qiuying Sha, et al.Annals of Human Genetics|May 1, 1990
Gaucher disease associated with a unique KpnI restriction site: identification of the amino-acid substitutionE Beutler, T GelbartAnnals of Human Genetics|August 21, 2009
The late Pleistocene colonization of South America: an interdisciplinary perspectiveFrancisco Rothhammer, Tom D DillehayAnnals of Human Genetics|January 1, 1991
Multiple recombination events are responsible for the heterogeneity of alpha(+)-thalassemia haplotypes among the forest tribes of Andhra Pradesh, IndiaR Fodde, C L Harteveld, M Losekoot, et al.Annals of Human Genetics|August 24, 2010
Phylogeography of the Y-chromosome haplogroup C in northern EurasiaBoris Malyarchuk, Miroslava Derenko, Galina Denisova, et al.Pageof 231