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Human Genetics|June 6, 2016
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21Craig C Teerlink, Daniel Leongamornlert, Tokhir Dadaev, et al.
American Journal of Human Genetics|September 27, 2016
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense VariantsNilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, et al.
European Urology Oncology|January 13, 2021
Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium StudyQuesta Karlsson, Mark N Brook, Tokhir Dadaev, et al.
Human Molecular Genetics|May 5, 2007
Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer GeneticsNicola J Camp, Lisa A Cannon-Albright, James M Farnham, et al.
BMC Medical Genetics|June 21, 2012
Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) familiesJoan E Bailey-Wilson, Erica J Childs, Cheryl D Cropp, et al.
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