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Circulation. Cardiovascular Genetics|December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskBing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
The Journal of Clinical Investigation|November 29, 2016
Biallelic mutations in IRF8 impair human NK cell maturation and functionEmily M Mace, Venetia Bigley, Justin T Gunesch, et al.
Plos One|September 27, 2007
Paradoxical DNA repair and peroxide resistance gene conservation in Bacillus pumilus SAFR-032Jason Gioia, Shailaja Yerrapragada, Xiang Qin, et al.
JAMA Oncology|January 30, 2016
Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid TumorsD Williams Parsons, Angshumoy Roy, Yaping Yang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 9, 2026
An integrated cardiometabolic genetic testing program in a predominantly Hispanic population within a community settingBo Yuan, Layla A Abushamat, Stacey Pereira, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2016
Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative geneMir Reza Bekheirnia, Nasim Bekheirnia, Matthew N Bainbridge, et al.
Blood|April 11, 2018
Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosisIvan K Chinn, Olive S Eckstein, Erin C Peckham-Gregory, et al.
Cancer Discovery|August 24, 2022
Proteogenomic Markers of Chemotherapy Resistance and Response in Triple-Negative Breast CancerMeenakshi Anurag, Eric J Jaehnig, Karsten Krug, et al.
Cell Reports|March 8, 2016
Multilevel Genomics-Based Taxonomy of Renal Cell CarcinomaFengju Chen, Yiqun Zhang, Yasin Şenbabaoğlu, et al.
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