Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot
Donna J. Page(Manchester Metropolitan University), Bernard Keavney(Manchester Academic Health Science Centre), Elisavet Fotiou(Manchester Metropolitan University), Mathieu Bourgey(McGill University and Génome Québec Innovation Centre), Simon G. Williams(Manchester Metropolitan University), Martín Baron(Manchester Academic Health Science Centre), Matthieu J. Miossec(Manchester Metropolitan University), Louise Sutcliffe(Manchester Metropolitan University), Connie R. Bezzina(Amsterdam UMC Location University of Amsterdam), Jeroen Breckpot(KU Leuven), Richard M. Monaghan(Manchester Metropolitan University), Sally L. Dunwoodie(Victor Chang Cardiac Research Institute), Graham Stuart, Marc Gewillig(University Hospital Schleswig-Holstein), J. David Brook(University of Nottingham), Sanjeev S. Bhaskar(Manchester Metropolitan University), Robert Eveleigh(Manchester Metropolitan University), Graeme C. Black, Guillaume Bourque(McGill University), Kerry Setchfield(University of Nottingham), Mauro Santibanez‐Koref(Centre for Life), Alex V. Postma(University of Amsterdam), Ana Töpf(Newcastle upon Tyne Hospitals NHS Foundation Trust), Koenraad Devriendt(University Medical Center Groningen), William G. Newman(Manchester Metropolitan University), Barbara J.M. Mulder(Walsh University), Kathryn E. Hentges(Manchester Academic Health Science Centre), G.M. Lathrop(Emory University), Heather J. Cordell(Newcastle University), James R. Bentham(Manchester Metropolitan University), Shoumo Bhattacharya(Centre for Human Genetics), John O’Sullivan(The University of Sydney), Frances Bu’Lock(Glenfield Hospital), David S. Winlaw(Children's Hospital at Westmead)
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