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Annals of Human Genetics|September 24, 2010
MLH1 Differential allelic expression in mutation carriers and controlsMauro Santibanez Koref, Valerie Wilson, Nicola Cartwright, et al.Annals of Human Genetics|February 12, 2011
Association of polymorphisms in the solute carrier organic anion transporter family member 1B1 gene with essential hypertension in the Uyghur populationRong Lin, Xiaofeng Wang, Weichen Zhou, et al.Annals of Human Genetics|February 18, 2011
The association of a single-nucleotide polymorphism of the IL-2 inducible T-cell Kinase gene with asthmaShin-Hwa Lee, Hun Soo Chang, An-Soo Jang, et al.Annals of Human Genetics|February 2, 2011
A comparison of association methods correcting for population stratification in case-control studiesChengqing Wu, Andrew DeWan, Josephine Hoh, et al.Annals of Human Genetics|January 5, 2011
Genetic studies of Prader-Willi patients provide evidence for conservation of genomic architecture in proximal chromosome 15qAihua Hou, Shuan-Pei Lin, Shi Yun Ho, et al.Annals of Human Genetics|August 21, 2009
Founder effects for ATM gene mutations in Italian Ataxia Telangiectasia familiesLuciana Chessa, Maria Piane, Monia Magliozzi, et al.Annals of Human Genetics|April 14, 2010
Permutation and parametric bootstrap tests for gene-gene and gene-environment interactionsPetra Bůžková, Thomas Lumley, Kenneth RiceAnnals of Human Genetics|April 8, 2010
Association of genetic variants, ethnicity and preterm birth with amniotic fluid cytokine concentrationsRamkumar Menon, Stephen J Fortunato, Digna R Velez Edwards, et al.Annals of Human Genetics|July 22, 2010
An INSIG2 polymorphism affects glucose homeostasis in Sardinian obese children and adolescentsPatrizia Zavattari, Alberto Loche, Patrizia Civolani, et al.Annals of Human Genetics|July 21, 2010
Genetic variants in RELN are associated with otosclerosis in a non-European population from TunisiaAyda Khalfallah, Isabelle Schrauwen, Malek Mnaja, et al.Pageof 231