Showing results (871-880 of 1,165) with videos related to

Sort By:
Pageof 117
Nature|June 5, 2014
Novel somatic and germline mutations in intracranial germ cell tumoursLinghua Wang, Shigeru Yamaguchi, Matthew D Burstein, et al.
Nature Communications|June 1, 2016
Genome-culture coevolution promotes rapid divergence of killer whale ecotypesAndrew D Foote, Nagarjun Vijay, María C Ávila-Arcos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2015
Molecular diagnostic experience of whole-exome sequencing in adult patientsJennifer E Posey, Jill A Rosenfeld, Regis A James, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 2, 2018
MLH1-rheMac hereditary nonpolyposis colorectal cancer syndrome in rhesus macaquesDavid W Brammer, Patrick J Gillespie, Mei Tian, et al.
Annals of Clinical and Translational Neurology|April 15, 2020
Biallelic GRM7 variants cause epilepsy, microcephaly, and cerebral atrophyDana Marafi, Tadahiro Mitani, Sedat Isikay, et al.
American Journal of Human Genetics|March 5, 2016
Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar AtrophyTamar Harel, Gozde Yesil, Yavuz Bayram, et al.
Circulation. Arrhythmia and Electrophysiology|September 11, 2012
The study of antiarrhythmic medications in infancy (SAMIS): a multicenter, randomized controlled trial comparing the efficacy and safety of digoxin versus propranolol for prophylaxis of supraventricular tachycardia in infantsShubhayan Sanatani, James E Potts, John H Reed, et al.
Plos One|July 24, 2008
Novel microRNA candidates and miRNA-mRNA pairs in embryonic stem (ES) cellsPeili Gu, Jeffrey G Reid, Xiaolian Gao, et al.
Genome Medicine|November 2, 2016
Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomicsMaria Nicla Loviglio, Christine R Beck, Janson J White, et al.
The New England Journal of Medicine|October 4, 2013
Clinical whole-exome sequencing for the diagnosis of mendelian disordersYaping Yang, Donna M Muzny, Jeffrey G Reid, et al.
Pageof 117