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Annals of Human Genetics|February 3, 2009
Variants in intron 13 of the ELMO1 gene are associated with diabetic nephropathy in African AmericansT S Leak, P S Perlegas, S G Smith, et al.Annals of Human Genetics|December 2, 2008
A novel point variant in NTRK3, R645C, suggests a role of this gene in the pathogenesis of Hirschsprung diseaseR M Fernández, A Sánchez-Mejías, M D Mena, et al.Annals of Human Genetics|January 1, 1978
Segregation of ABO, AK1 and ACONs in families with abnormalities of chromosome 9P J Cook, E B Robson, K E Buckton, et al.Annals of Human Genetics|May 12, 2010
Analysis of RET, ZEB2, EDN3 and GDNF genomic rearrangements in central congenital hyperventilation syndrome patients by multiplex ligation-dependent probe amplificationAlexandre Serra, Heike Görgens, Karin Alhadad, et al.Annals of Human Genetics|June 10, 2010
Inferring haplotype/disease association by joint use of case-parents trios and case-parent pairsYue-Qing Hu, Ji-Yuan ZhouAnnals of Human Genetics|June 10, 2010
Influence of population stratification on population-based marker-disease association analysisTengfei Li, Zhaohai Li, Zhiliang Ying, et al.Annals of Human Genetics|September 21, 2006
Analysis of case-only studies accounting for genotyping errorK F ChengAnnals of Human Genetics|March 10, 2007
Confidence intervals for candidate gene effects and environmental factors in population-based association studies of familiesJaney Shin, Gerarda A Darlington, Cecilia Cotton, et al.Annals of Human Genetics|March 14, 2007
A two-stage approach to the correction of ascertainment bias in complex genetic studies involving variance componentsJ Bowden, J R Thompson, P R BurtonAnnals of Human Genetics|December 13, 2006
Common polymorphisms in the CACNA1H gene associated with childhood absence epilepsy in Chinese Han populationJ Liang, Y Zhang, Y Chen, et al.Pageof 231