Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease

Rachel Soemedi(Newcastle University), Ian Wilson(Newcastle University), Jamie Bentham(Centre for Human Genetics), Rebecca Darlay(Newcastle University), Ana Töpf(Newcastle University), Diana Zélénika(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Catherine Cosgrove(Centre for Human Genetics), Kerry Setchfield(University of Nottingham), Chris Thornborough(Glenfield Hospital), Javier T Granados-Riveron(University of Nottingham), Gillian M. Blue(Children's Hospital at Westmead), Jeroen Breckpot(KU Leuven), Stephen Hellens(Institute of Genetics and Cancer), Simon Zwolinkski(Institute of Genetics and Cancer), Elise Glen(Newcastle University), Chrysovalanto Mamasoula(Newcastle University), Thahira Rahman(Newcastle University), Darroch Hall(Newcastle University), Anita Rauch(University of Zurich), Koenraad Devriendt(KU Leuven), Marc Gewillig(KU Leuven), John O’ Sullivan(National Health Service), David S. Winlaw(Children's Hospital at Westmead), Frances Bu’Lock(Glenfield Hospital), J. David Brook(University of Nottingham), Shoumo Bhattacharya(Centre for Human Genetics), Mark Lathrop(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Mauro Santibanez‐Koref(Newcastle University), Heather J. Cordell(Newcastle University), Judith A. Goodship(Newcastle University), Bernard Keavney(Newcastle University)
The American Journal of Human Genetics
August 30, 2012
Cited by 338Open Access
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