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Human Genetics|July 1, 2008
Replication of association between ELAVL4 and Parkinson disease: the GenePD studyAnita L DeStefano, Jeanne Latourelle, Mark F Lew, et al.
Human Genetics|July 27, 2007
In vitro and ex vivo suppression by aminoglycosides of PCDH15 nonsense mutations underlying type 1 Usher syndromeAnnie Rebibo-Sabbah, Igor Nudelman, Zubair M Ahmed, et al.
Human Genetics|September 24, 2008
Association between Apolipoprotein E genotype and cerebral palsy is not confirmed in a Caucasian populationGai L McMichael, Catherine S Gibson, Paul N Goldwater, et al.
Human Genetics|September 24, 2008
The clinical characteristics of Werner syndrome: molecular and biochemical diagnosisMeltem Muftuoglu, Junko Oshima, Cayetano von Kobbe, et al.
Human Genetics|November 27, 2008
Lactose digestion and the evolutionary genetics of lactase persistenceCatherine J E Ingram, Charlotte A Mulcare, Yuval Itan, et al.
Human Genetics|May 1, 1991
Carrier detection in haemophilia A by direct analysis of factor VIII gene lesionsD S Millar, P J Green, B Zoll, et al.
Human Genetics|November 28, 2008
The association of SNPs in ADIPOQ, ADIPOR1, and ADIPOR2 with insulin sensitivity in a cohort of adolescents and their parentsLaura J Rasmussen-Torvik, James S Pankow, David R Jacobs, et al.
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