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JCO Precision Oncology|January 7, 2022
Clinical Implications of Pathogenic Germline Variants in Small Intestine Neuroendocrine Tumors (SI-NETs)Kimberly Perez, Matthew H Kulke, Anu Chittenden, et al.
European Heart Journal|September 24, 2021
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic deathRoddy Walsh, Arnon Adler, Ahmad S Amin, et al.
Circulation|January 28, 2020
An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT SyndromeArnon Adler, Valeria Novelli, Ahmad S Amin, et al.
Journal of the American Heart Association|August 30, 2021
ATP1A3-Encoded Sodium-Potassium ATPase Subunit Alpha 3 D801N Variant Is Associated With Shortened QT Interval and Predisposition to Ventricular Fibrillation Preceded by BradycardiaMary E Moya-Mendez, Chiagoziem Ogbonna, Jordan E Ezekian, et al.
Human Mutation|June 10, 2020
An assessment of the role of vinculin loss of function variants in inherited cardiomyopathyMegan H Hawley, Naif Almontashiri, Leslie G Biesecker, et al.
ACS Applied Materials & Interfaces|October 5, 2021
Photocatalytic Mechanism Control and Study of Carrier Dynamics in CdS@C3N5 Core-Shell NanowiresKazi M Alam, Charles E Jensen, Pawan Kumar, et al.
American Journal of Medical Genetics. Part A|June 24, 2020
Estimating the relative frequency of leukodystrophies and recommendations for carrier screening in the era of next-generation sequencingJohanna L Schmidt, Amy Pizzino, Jessica Nicholl, et al.
Global Change Biology. Bioenergy|March 24, 2017
Bioenergy production and sustainable development: science base for policymaking remains limitedCarmenza Robledo-Abad, Hans-Jörg Althaus, Göran Berndes, et al.
Human Mutation|October 13, 2018
ClinVar database of global familial hypercholesterolemia-associated DNA variantsMichael A Iacocca, Joana R Chora, Alain Carrié, et al.
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