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Human Heredity|October 24, 2006
A module map showing interaction between apolipoprotein E and phospholipase A2 polymorphism in lipid profilesFor-Wey Lung, Wei-Tsung Kao, Bih-Ching Shu, et al.Human Heredity|October 22, 2008
Heritability of lung function in severe alpha-1 antitrypsin deficiencyD L DeMeo, E J Campbell, M L Brantly, et al.Human Heredity|October 22, 2008
Optimal DNA pooling-based two-stage designs in case-control association studiesYihong Zhao, Shuang WangHuman Heredity|January 1, 1991
Population genetics of alpha-1-antitrypsin polymorphism in US whites, US blacks and African blacksS DeCroo, M I Kamboh, R E FerrellHuman Heredity|January 1, 1991
Polymorphisms of serum proteins in Japanese patients with vascular diseases. I. Factor XIIIB, plasminogen and complement types in primary varicose veinsK Mizutani, H Nishimukai, T Yasugi, et al.Human Heredity|June 13, 2009
Methods for assessing familial aggregation: family history measures and confounding in the standard cohort, reconstructed cohort and case-control designsRegina Zimmerman, Deb K Pal, Adrienne Tin, et al.Human Heredity|January 28, 2009
Variance components linkage analysis with repeated measurementsLiming Liang, Wei-Min Chen, Pak C Sham, et al.Human Heredity|October 16, 2010
Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired familiesTabatha R Simmons, Judy F Flax, Marco A Azaro, et al.Human Heredity|April 19, 2013
Using affected sib-pairs to uncover rare disease variantsHervé Perdry, Bertram Müller-Myhsok, Françoise Clerget-DarpouxHuman Heredity|April 19, 2013
Does accounting for gene-environment interactions help uncover association between rare variants and complex diseases?Rémi Kazma, Niall J Cardin, John S WittePageof 237