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The Journal of Invasive Cardiology|December 20, 2021
The Single-Access Technique for Impella Protected Percutaneous Coronary Intervention: A Single-Center ExperienceGanesh Gajanan, Yiannis S Chatzizisis, Edward O'Leary, et al.European Journal of Human Genetics : EJHG|September 20, 2012
EMQN/CMGS best practice guidelines for the molecular genetic testing of Huntington diseaseMonique Losekoot, Martine J van Belzen, Sara Seneca, et al.European Journal of Human Genetics : EJHG|April 14, 2019
Managing uncertainty in inherited cardiac pathologies-an international multidisciplinary surveyTerri Patricia McVeigh, Luke J Kelly, Elizabeth Whitmore, et al.Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|September 2, 2022
Predictors of high-degree atrioventricular block in patients with new-onset left bundle branch block following transcatheter aortic valve replacementNashwa M Abdulsalam, Jeanne E Poole, Elizabeth R Lyden, et al.European Journal of Human Genetics : EJHG|November 4, 2004
Uroplakin III is not a major candidate gene for primary vesicoureteral refluxHelena Kelly, Sean Ennis, Akihiro Yoneda, et al.American Journal of Medical Genetics. Part A|February 4, 2017
Incidence of Fragile X syndrome in IrelandJames J O'Byrne, Michael Sweeney, Deirdre E Donnelly, et al.Archives of Neurology|February 15, 2002
Intrafamilial phenotypic variability in Friedreich ataxia associated with a G130V mutation in the FRDA geneDominick J H McCabe, Nicholas W Wood, Fergus Ryan, et al.Human Mutation|June 20, 2003
Comparison of the CFTR mutation spectrum in three cohorts of patients of Celtic origin from Brittany (France) and IrelandVirginie Scotet, David E Barton, James B G Watson, et al.European Journal of Human Genetics : EJHG|May 19, 2011
Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromesJennifer Boyle, Malcolm Hawkins, David E Barton, et al.European Journal of Human Genetics : EJHG|June 3, 2020
National Newborn Screening for cystic fibrosis in the Republic of Ireland: genetic data from the first 6.5 yearsErina Sasaki, Marija Kostocenko, Niamh Lang, et al.Pageof 4