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American Journal of Human Genetics|July 1, 1989
Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneityU Francke, B T Darras, J H Hersh, et al.
American Journal of Human Genetics|March 1, 1989
Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite BrethrenT M Fujiwara, K Morgan, R H Schwartz, et al.
American Journal of Human Genetics|March 1, 1989
Polymorphic DNA haplotypes at the LDL receptor locusE Leitersdorf, A Chakravarti, H H Hobbs
American Journal of Human Genetics|February 3, 2015
Gene expression in transformed lymphocytes reveals variation in endomembrane and HLA pathways modifying cystic fibrosis pulmonary phenotypesWanda K O'Neal, Paul Gallins, Rhonda G Pace, et al.
American Journal of Human Genetics|September 21, 2021
Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk geneLu Qiao, Le Xu, Lan Yu, et al.
American Journal of Human Genetics|December 1, 1986
Genetic analysis of cystic fibrosis using linked DNA markersL C Tsui, K Buetow, M Buchwald
American Journal of Human Genetics|April 14, 2022
Leveraging LD eigenvalue regression to improve the estimation of SNP heritability and confounding inflationShuang Song, Wei Jiang, Yiliang Zhang, et al.
American Journal of Human Genetics|July 1, 1975
Cytidine deaminase: a new genetic polymorphism demonstrated in human granulocytesY S Teng, J E Anderson, E R Giblett
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