Genetic variants in the <i>KDM6B</i> gene are associated with neurodevelopmental delays and dysmorphic features

Elliot Stolerman(Greenwood Genetic Center), Raymond J. Louie(Greenwood Genetic Center), Boris Keren(Sorbonne Université), Grazia M.S. Mancini(Erasmus MC), Lauren O’Grady(Massachusetts General Hospital), Petra Zwijnenburg(Hospitais da Universidade de Coimbra), Ingrid M. Wentzensen, Quinten Waisfisz(University Medical Center Utrecht), Caroline Nava(Centre National de la Recherche Scientifique), Julie R. Jones(Greenwood Genetic Center), Inderneel Sahai(Massachusetts General Hospital), Luis Escobar(St. Vincent Hospital), Marjon van Slegtenhorst(Erasmus MC), Yves Lacassie(Children's Hospital of New Orleans), Jennifer Keller‐Ramey, R. Frank Kooy(University of Antwerp), Meral Gunay‐Aygun(Johns Hopkins University), Jennifer L. Stallworth(Greenwood Genetic Center), Fatima Almusafri(Hamad Medical Corporation), Marije Meuwissen(Antwerp University Hospital), Bénédicte Héron(Délégation Paris 5), Edwin Reyniers(University of Antwerp), Kirsty McWalter, Kristin G. Monaghan, Ron Hochstenbach(Amsterdam University Medical Centers), E. Nicolás Francisco(Greenwood Genetic Center), Delphine Héron(Sorbonne Université), Barbara K. Burton(Women & Children's Hospital of Buffalo), Katherine Kim(Ithaka Harbors), Richard Person(GenVec), Krista Schatz(Johns Hopkins University)
American Journal of Medical Genetics Part A
May 23, 2019
Cited by 54


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