Weaver syndrome and <i>EZH2</i> mutations: Clarifying the clinical phenotype
Katrina Tatton‐Brown(St George’s University Hospitals NHS Foundation Trust), Nazneen Rahman(Institute of Cancer Research), Shelagh Joss(Oulu University Hospital), I. Karen Temple(University of Southampton), 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 and Children’s NHS Foundation Trust), Volker Strenger(Medical University of Graz), Clare Taylor(Birmingham City University), Sandra Hanks(Institute of Cancer Research), Lionel Van Maldergem, Tom Cushing(University of New Mexico), Vivienne McConnell(University of Ulster), Siddharth Banka(University of Manchester), 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(University College Dublin), Keiichi Ozono(Osaka Gakuin University), 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(Hôpital Necker-Enfants Malades), Julia Rankin(Royal Devon & Exeter NHS Foundation Trust), Marie‐Line Jacquemont(Assistance Publique – Hôpitaux de Paris)
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