Weaver syndrome and <i>EZH2</i> mutations: Clarifying the clinical phenotype
Katrina Tatton‐Brown(Institute of Cancer Research), Nazneen Rahman(Royal Marsden NHS Foundation Trust), Shelagh Joss(Oulu University Hospital), I. Karen Temple(Princess Anne Hospital), Kyra E. Stuurman(Amsterdam UMC Location Vrije Universiteit Amsterdam), Lynne M. Bird(University of California San Diego), Ana Medeira(Hospital de Santa Maria), Anne R. Murray(Institute of Cancer Research), Miranda Splitt(Newcastle upon Tyne Hospital), Hannah Titheradge(Birmingham Women's Hospital), Volker Strenger(Medical University of Graz), Clare Taylor(University of Oxford), Sandra Hanks(Institute of Cancer Research), Lionel Van Maldergem, Tom Cushing(University of New Mexico), Vivienne McConnell(University of Ulster), Siddharth Banka(Manchester Academic Health Science Centre), Debbie Shears(Churchill Hospital), Carol L. Clericuzio(Medical University of South Carolina), Marleen Simon(Erasmus University Rotterdam), Esther Kinning(University Medical Center Groningen), Frances Flinter(Guy's and St Thomas' NHS Foundation Trust), Sally Ann Lynch(Temple Street Children's University Hospital), Keiichi Ozono(The University of Osaka), Trevor Cole(Birmingham Women's Hospital), Sheila Seal(Institute of Cancer Research), Alex Magee(University of Ulster), Jenny Douglas(Institute of Cancer Research), Michael A. Patton(St George's Hospital), Ruth Armstrong(Addenbrooke's Hospital), Valérie Cormier‐Daire(Institut Necker Enfants Malades), Julia Rankin(Royal Devon & Exeter NHS Foundation Trust), Marie‐Line Jacquemont(Assistance Publique – Hôpitaux de Paris)
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