Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease
Rachel Soemedi(Newcastle University), Bernard Keavney(Manchester Academic Health Science Centre), Simon Zwolinkski(Institute of Genetics and Cancer), Jeroen Breckpot(KU Leuven), Marc Gewillig(KU Leuven), Jamie Bentham(University of Oxford), J. David Brook(University of Nottingham), Rebecca Darlay(Newcastle University), Gillian M. Blue(Children's Hospital at Westmead), Anita Rauch(University of Zurich), Ian Wilson(Newcastle University), Chrysovalanto Mamasoula(Centro de Investigación en Red en Enfermedades Cardiovasculares), Kerry Setchfield(University of Nottingham), Mauro Santibanez‐Koref(Newcastle University), Javier T Granados-Riveron(University of Nottingham), Stephen Hellens(Institute of Genetics and Cancer), Ana Töpf(NIHR Newcastle Biomedical Research Centre), Koenraad Devriendt(Universitair Ziekenhuis Leuven), Diana Zélénika(Centre National de Recherche en Génomique Humaine), Heather J. Cordell(Newcastle University), Shoumo Bhattacharya(Centre for Human Genetics), Chris Thornborough(Glenfield Hospital), Frances Bu’Lock(Glenfield Hospital), Darroch Hall(Newcastle University), Catherine Cosgrove(University of Oxford), Judith A. Goodship(Newcastle University), John O’ Sullivan(National Health Service), Thahira Rahman(Centre for Life), David S. Winlaw(Lurie Children's Hospital), Mark Lathrop(McGill Genome Centre), Elise Glen(Newcastle University)
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