Showing results (1201-1210 of 1,235) with videos related to

Sort By:
Pageof 124
The Lancet. HIV|August 9, 2021
Improving health equity and ending the HIV epidemic in the USA: a distributional cost-effectiveness analysis in six citiesAmanda My Linh Quan, Cassandra Mah, Emanuel Krebs, et al.
Annals of Internal Medicine|October 22, 2019
Management of Nonvariceal Upper Gastrointestinal Bleeding: Guideline Recommendations From the International Consensus GroupAlan N Barkun, Majid Almadi, Ernst J Kuipers, et al.
American Journal of Human Genetics|January 24, 2012
Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndromePhilippe M Campeau, Jaeseung C Kim, James T Lu, et al.
Journal of Inherited Metabolic Disease|January 18, 2023
Fractionated plasma N-glycan profiling of novel cohort of ATP6AP1-CDG subjects identifies phenotypic associationHana Alharbi, Earnest James Paul Daniel, Jenny Thies, et al.
American Journal of Human Genetics|March 5, 2013
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycanElizabeth Stevens, Keren J Carss, Sebahattin Cirak, et al.
Digestive Diseases and Sciences|October 20, 2022
Existing Bowel Preparation Quality Scales Are Reliable in the Setting of Centralized Endoscopy ReadingJurij Hanzel, Michael Sey, Christopher Ma, et al.
Molecular Genetics and Metabolism|March 17, 2020
Successful liver transplantation in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)KimberlyA Kripps, Warapan Nakayuenyongsuk, Brian J Shayota, et al.
Genetics and Molecular Research : GMR|March 25, 2017
SNP detection using RNA-sequences of candidate genes associated with puberty in cattleM M Dias, A Cánovas, C Mantilla-Rojas, et al.
Water Research|February 28, 2012
Spatial and temporal variation in indicator microbe sampling is influential in beach management decisionsAmber A Enns, Laura J Vogel, Amir M Abdelzaher, et al.
American Journal of Human Genetics|September 13, 2016
De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive DysmorphismsKarin Weiss, Paulien A Terhal, Lior Cohen, et al.
Pageof 124