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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 <Title>Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype</Title>

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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