Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome

J. K. J. VAN HOUDT(KU Leuven), Joris Vermeesch(KU Leuven), Eve Seuntjens(VIB-KU Leuven Center for Brain & Disease Research), Nora Shannon(Nottingham City Hospital), Małgorzata Krajewska‐Walasek(Children's Memorial Health Institute), Irene Stolte‐Dijkstra(University of Groningen), Annick Vogels(KU Leuven), Bryan D. Hall(University of Kentucky), Livia Garavelli(Azienda Sanitaria Unità Locale di Reggio Emilia), Simone Gana(University of Pavia), Catheline Vilain(Université Libre de Bruxelles), Elizabeth C. Rosser(University College of Osteopathy), Danny Huylebroeck(Erasmus MC), Marco Castori(Unknown), Yves Moreau(KU Leuven), Alejandro Sifrim(KU Leuven), Matthew A. Deardorff(Children's Hospital of Philadelphia), Fanny Morice‐Picard(Hôpital Saint-André), Denise Horn(Humboldt-Universität zu Berlin), Beata Nowakowska(Mother and Child Foundation), Shane McKee(Belfast City Hospital), Raoul C. M. Hennekam(University of Amsterdam), Orsetta Zuffardi(University of Pavia), Jacek Pilch(Medical University of Silesia), Isabel Filges(University Children’s Hospital Basel), Dagmar Wieczorek(Essen University Hospital), Antoine H. C. van Kampen(Academic Medical Center), Koenraad Devriendt(Universitair Ziekenhuis Leuven), Barbera D. C. van Schaik(Academic Medical Center), Matthew A. Lines(Children's Hospital of Eastern Ontario), Jakub Klapecki, Emma Wakeling(Northwick Park Hospital), Armand Bottani(University Hospital of Geneva), Ewa Obersztyn, Patrick Van Dijck(Institute of Philosophy), de Man(Amphia Ziekenhuis), Louise C. Wilson(Great Ormond Street Hospital for Children NHS Foundation Trust), Omar Abdul‐Rahman(Cornell University), Sérgio B. Sousa, Saskia M. Maas(Academic Medical Center), Alex Magee(University of Ulster), Alan Fryer(University of Liverpool), Kay MacDermot(Wessex Regional Genetics Laboratory), Gabriele Gillessen‐Kaesbach(University Hospital Schleswig-Holstein), Alma Kuechler(Essen University Hospital), Jean‐Pierre Fryns(KU Leuven), Valérie Cormier‐Daire(Hôpital Necker-Enfants Malades), Marie-José H. van den Boogaard(University Medical Center Utrecht), Nelson Avonce(Universidad Autónoma del Estado de Morelos)
Nature Genetics
February 26, 2012
Cited by 244


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