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American Journal of Human Genetics|April 5, 2008
On the replication of genetic associations: timing can be everything!Jessica Lasky-Su, Helen N Lyon, Valur Emilsson, et al.
American Journal of Human Genetics|April 9, 2008
A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian familyFatemeh Alasti, Abdorrahim Sadeghi, Mohammad Hossein Sanati, et al.
American Journal of Human Genetics|April 9, 2008
Mapping of small RNAs in the human ENCODE regionsChristelle Borel, Maryline Gagnebin, Corinne Gehrig, et al.
American Journal of Human Genetics|February 7, 2008
Neocentromeres: new insights into centromere structure, disease development, and karyotype evolutionOwen J Marshall, Anderly C Chueh, Lee H Wong, et al.
American Journal of Human Genetics|February 7, 2008
Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synucleinGaofeng Wang, Joelle M van der Walt, Gregory Mayhew, et al.
American Journal of Human Genetics|February 7, 2008
A unified association analysis approach for family and unrelated samples correcting for stratificationXiaofeng Zhu, Shengchao Li, Richard S Cooper, et al.
American Journal of Human Genetics|February 7, 2008
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardationGuy Froyen, Mark Corbett, Joke Vandewalle, et al.
American Journal of Human Genetics|February 7, 2008
Basal laminar drusen caused by compound heterozygous variants in the CFH geneCamiel J F Boon, B Jeroen Klevering, Carel B Hoyng, et al.
American Journal of Human Genetics|April 22, 2008
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndromeDaniel F Schorderet, Olivia Nichini, Gaëlle Boisset, et al.
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