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1 Ergebnisse
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Weaver syndrome and EZH2 mutations: Clarifying the clinical..:
Tatton‐Brown, Katrina
;
Murray, Anne
;
Hanks, Sandra
...
American Journal of Medical Genetics Part A. 161 (2013) 12 - p. 2972-2980 , 2013
Link:
https://doi.org/10.1002/ajmg.a.36229
RT Journal T1
Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.36229&Exemplar=1&LAN=DE A1 Tatton‐Brown, Katrina A1 Murray, Anne A1 Hanks, Sandra A1 Douglas, Jenny A1 Armstrong, Ruth A1 Banka, Siddharth A1 Bird, Lynne M. A1 Clericuzio, Carol L. A1 Cormier‐Daire, Valerie A1 Cushing, Tom A1 Flinter, Frances A1 Jacquemont, Marie‐Line A1 Joss, Shelagh A1 Kinning, Esther A1 Lynch, Sally Ann A1 Magee, Alex A1 McConnell, Vivienne A1 Medeira, Ana A1 Ozono, Keiichi A1 Patton, Michael A1 Rankin, Julia A1 Shears, Debbie A1 Simon, Marleen A1 Splitt, Miranda A1 Strenger, Volker A1 Stuurman, Kyra A1 Taylor, Clare A1 Titheradge, Hannah A1 Van Maldergem, Lionel A1 Temple, I. Karen PB Wiley YR 2013 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 161 IS 12 SP 2972 OP 2980 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.36229 DO https://doi.org/10.1002/ajmg.a.36229 SF ELIB - SuUB Bremen
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