Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in theZEB2gene-Reference-Cited by-同舟云学术

Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in theZEB2gene

Published:2008-12-01 Issue:23 Volume:146A Page:3095-3099
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Cecconi Massimiliano,Forzano Francesca,Garavelli Livia,Pantaleoni Chiara,Grasso Marina,Dagna Bricarelli Franca,Perroni Lucia,Di Maria Emilio,Faravelli Francesca

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference10 articles.

1. Clinical features and management issues in Mowat-Wilson syndrome;Adam;Am J Med Genet Part A,2006

2. Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease;Cacheux;Hum Mol Genet,2001

3. ZFHX1B mutations in patients with Mowat-Wilson syndrome;Dastot-Le Moal;Hum Mutat,2007

4. Mowat-Wilson syndrome;Garavelli;Orphanet J Rare Dis,2007

5. Recurrence of Mowat-Wilson syndrome in siblings with the same proven mutation;McGaughran;Am J Med Genet Part A,2005

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