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Human Molecular Genetics|June 1, 2011
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disordersChristian P Schaaf, Aniko Sabo, Yasunari Sakai, et al.Nature Communications|December 2, 2010
Deep resequencing reveals excess rare recent variants consistent with explosive population growthAlex Coventry, Lara M Bull-Otterson, Xiaoming Liu, et al.The New England Journal of Medicine|November 13, 2014
Inactivating mutations in NPC1L1 and protection from coronary heart disease, Nathan O Stitziel, Hong-Hee Won, et al.The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.Pageof 1