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Journal of Cardiovascular Electrophysiology|May 23, 2013
Mutation location effect on severity of phenotype during exercise testing in type 1 long-QT syndrome: impact of transmembrane and C-loop locationZachary W M Laksman, Robert M Hamilton, Priya Chockalingam, et al.
American Journal of Medical Genetics. Part A|November 18, 2008
Predictive genetic testing for cardiovascular diseases: impact on carrier childrenTineke M Meulenkamp, Aad Tibben, Eline D Mollema, et al.
Heart Rhythm|April 4, 2020
SARS-CoV-2, COVID-19, and inherited arrhythmia syndromesCheng-I Wu, Pieter G Postema, Elena Arbelo, et al.
Computers in Biology and Medicine|February 19, 2021
Improving electrocardiogram-based detection of rare genetic heart disease using transfer learning: An application to phospholamban p.Arg14del mutation carriersRicardo R Lopes, Hidde Bleijendaal, Lucas A Ramos, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Somatic mosaicism contributes to phenotypic variation in Timothy syndromeSusan P Etheridge, Neil E Bowles, Cammon B Arrington, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|February 7, 2024
Is it safe to give birth with an activated implantable cardioverter-defibrillator: A multicentre observational studyWilleke van der Stuijt, Kirsten M Kooiman, Jolien A de Veld, et al.
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