Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype

Tatton-Brown, Katrina ; Murray, Anne ; Hanks, Sandra ; Douglas, Jenny ; Armstrong, Ruth ; Banka, Siddharth ; Bird, Lynne M. ; Clericuzio, Carol L. ; Cormier-Daire, Valerie ; Cushing, Tom ; Flinter, Frances ; Jacquemont, Marie-Line ; Joss, Shelagh ; Kinning, Esther ; Lynch, Sally Ann ; Magee, Alex ; McConnell, Vivienne ; Medeira, Ana ; Ozono, Keiichi ; Patton, Michael ; Rankin, Julia ; Shears, Debbie ; Simon, Marleen ; Splitt, Miranda ; Strenger, Volker ; Stuurman, Kyra ; Taylor, Clare ; Titheradge, Hannah ; Van Maldergem, Lionel ; Temple, I. Karen ; Cole, Trevor ; Seal, Sheila ; Rahman, Nazneen

American journal of medical genetics. Part A, 2013-12, Vol.161A (12), p.2972-2980 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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