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American Journal of Human Genetics|May 16, 2009
DYNC2H1 mutations cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type IIINathalie Dagoneau, Marie Goulet, David Geneviève, et al.
American Journal of Preventive Medicine|December 20, 2017
U.S. Preventive Services Task Force Methods to Communicate and Disseminate Clinical Preventive Services RecommendationsAnn E Kurth, Alex H Krist, Amanda E Borsky, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 13, 2019
Null variants and deletions in BRWD3 cause an X-linked syndrome of mild-moderate intellectual disability, macrocephaly, and obesity: A series of 17 patientsPhilip J Ostrowski, Anna Zachariou, Chey Loveday, et al.
Clinical Genetics|January 23, 2019
Deep phenotyping of 14 new patients with IQSEC2 variants, including monozygotic twins of discordant phenotypeJessica A Radley, Rory B G O'Sullivan, Sarah E Turton, et al.
JAMA|January 28, 2016
Screening for Depression in Adults: US Preventive Services Task Force Recommendation StatementAlbert L Siu, , Kirsten Bibbins-Domingo, et al.
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