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Human Genetics|October 9, 2014
Testing evolutionary models of senescence: traditional approaches and future directionsChloe Robins, Karen N ConneelyHuman Genetics|August 18, 2014
Using familial information for variant filtering in high-throughput sequencing studiesMelanie Bahlo, Rick Tankard, Vesna Lukic, et al.Human Genetics|May 1, 1989
The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11J K Cowell, R B Wadey, B B Buckle, et al.Human Genetics|November 7, 2014
Loss-of-function mutation in the X-linked TBX22 promoter disrupts an ETS-1 binding site and leads to cleft palateXiazhou Fu, Yibin Cheng, Jia Yuan, et al.Human Genetics|January 1, 1989
Centromeric association and non-random distribution of centromeres in human tumour cellsT Haaf, M SchmidHuman Genetics|November 9, 2014
An argument for mechanism-based statistical inference in cancerDonald Geman, Michael Ochs, Nathan D Price, et al.Human Genetics|June 18, 2016
Differential frequency of NKG2C/KLRC2 deletion in distinct African populations and susceptibility to Trachoma: a new method for imputation of KLRC2 genotypes from SNP genotyping dataAdriana Goncalves, Pateh Makalo, Hassan Joof, et al.Human Genetics|July 3, 2016
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2Lyndal Henden, Saskia Freytag, Zaid Afawi, et al.Human Genetics|July 5, 2016
Whole-genome sequencing in French Canadians from QuebecCécile Low-Kam, David Rhainds, Ken Sin Lo, et al.Human Genetics|July 1, 1989
Chromosomal localization of human glutathione transferase genes of classes alpha, mu and piM Q Islam, A Platz, J Szpirer, et al.Pageof 958