Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls
Rachel Soemedi(Newcastle University), Bernard Keavney(Manchester Academic Health Science Centre), Jeroen Breckpot(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(Friedrich-Alexander-Universität Erlangen-Nürnberg), Ian Wilson(Newcastle University), Michael Hofbeck(University Children's Hospital Tübingen), Kerry Setchfield(University of Nottingham), Mauro Santibanez‐Koref(Newcastle University), Javier T Granados-Riveron(University of Nottingham), Matthew E. Hurles(Wellcome Sanger Institute), Ana Töpf(NIHR Newcastle Biomedical Research Centre), Koenraad Devriendt(University Medical Center Groningen), Ni Huang(Shanghai Jiao Tong University), 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), Thahira Rahman(Centre for Life), David S. Winlaw(Children's Hospital at Westmead), Mark Lathrop(McGill Genome Centre), Elise Glen(Newcastle University)
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