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Journal of Personalized Medicine|February 25, 2022
Discerning the Ambiguous Role of Missense <i>TTN</i> Variants in Inherited Arrhythmogenic SyndromesEstefanía Martínez-Barrios, Georgia Sarquella-Brugada, Alexandra Pérez-Serra, et al.Human Genetics|September 21, 2021
Clinical impact of rare variants associated with inherited channelopathies: a 5-year updateGeorgia Sarquella-Brugada, Anna Fernandez-Falgueras, Sergi Cesar, et al.Journal of Personalized Medicine|March 3, 2021
Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years LaterMarta Vallverdú-Prats, Mireia Alcalde, Georgia Sarquella-Brugada, et al.International Journal of Legal Medicine|January 24, 2023
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohortEstefanía Martinez-Barrios, Georgia Sarquella-Brugada, Alexandra Perez-Serra, et al.Forensic Science International. Genetics|April 6, 2020
Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?Jesus Mates, Irene Mademont-Soler, Anna Fernandez-Falgueras, et al.Pageof 7