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Annals of Human Genetics|November 2, 2019
Application of targeted exome and whole-exome sequencing for Chinese families with Stargardt diseaseHandong Dan, Xin Huang, Yiqiao Xing, et al.Annals of Human Genetics|June 19, 2021
Gene-based association analysis identified a novel gene associated with systemic lupus erythematosusXian Ding, Minglong Cai, Sun Wang, et al.Annals of Human Genetics|November 21, 2012
Impact on modes of inheritance and relative risks of using extreme sampling when designing genetic association studiesGang Zheng, Xu Jinfeng, Ao Yuan, et al.Annals of Human Genetics|January 31, 2013
Initial assessment of the pathogenic mechanisms of the recently identified Alzheimer risk LociPatrick Holton, Mina Ryten, Michael Nalls, et al.Annals of Human Genetics|February 1, 2013
A likelihood ratio test for genome-wide association under genetic heterogeneityMeng Qian, Yongzhao ShaoAnnals of Human Genetics|July 13, 2013
C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson diseaseKaren Nuytemans, Güney Bademci, Martin M Kohli, et al.Annals of Human Genetics|August 14, 2013
A genome-wide search for type 2 diabetes susceptibility genes in an extended Arab familyHabiba S Al Safar, Heather J Cordell, Osman Jafer, et al.Annals of Human Genetics|June 22, 2013
Common variants in KCNQ1 confer increased risk of type 2 diabetes and contribute to the diabetic epidemic in East Asians: a replication and meta-analysisHaoran Wang, Kun Miao, Jinzhao Zhao, et al.Annals of Human Genetics|January 1, 1990
Comparison of simple and modified Bernstein's methods in estimation of recessive allele frequency in the HLA systemJ M NamPageof 231