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Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype

Lookup NU author(s): Professor Sir John BurnORCiD, Dr Miranda Splitt



This is the final published version of an article that has been published in its final definitive form by John Wiley & Sons, Inc., 2013.

For re-use rights please refer to the publisher's terms and conditions.

Publication metadata

Author(s): Tatton-Brown K, Murray A, Hanks S, Douglas J, Armstrong R, Banka S, Bird LM, Clericuzio CL, Cormier-Daire V, Cushing T, Flinter F, Jacquemont ML, Jos S, Kinning E, Lynch SA, Magee A, McConnell V, Medeira A, Ozono K, Patton M, Rankin J, Shears D, Simon M, Splitt M, Strenger V, Stuurman K, Taylor C, Titheradge H, Van-Maldergem L, Temple IK, Cole T, Seal S

Publication type: Article

Publication status: Published

Journal: American Journal of Medical Genetics: Part A

Year: 2013

Volume: 161

Issue: 12

Pages: 2972-2980

Print publication date: 01/12/2013

Online publication date: 08/11/2013

Date deposited: 14/11/2016

ISSN (print): 1552-4825

ISSN (electronic): 1552-4833

Publisher: John Wiley & Sons, Inc.


DOI: 10.1002/ajmg.a.36229


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