Author:
Spaggiari Emmanuel,Baumann Clarisse,Alison Marianne,Oury Jean-François,Belarbi Nadia,Dupont Céline,Guimiot Fabien,Delezoide Anne-Lise
Subject
Genetics(clinical),Genetics,General Medicine
Reference16 articles.
1. Mowat–Wilson syndrome;Mowat;J. Med. Genet.,2003
2. Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22–q23;Mowat;J. Med. Genet.,1998
3. Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease;Wakamatsu;Nat. Genet.,2001
4. Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease;Cacheux;Hum. Mol. Genet.,2001
5. Mowat–Wilson syndrome;Mowat,2010
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