Mice Lacking Zfhx1b, the Gene That Codes for Smad-Interacting Protein-1, Reveal a Role for Multiple Neural Crest Cell Defects in the Etiology of Hirschsprung Disease–Mental Retardation Syndrome
- 1 February 2003
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 72 (2), 465-470
- https://doi.org/10.1086/346092
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- “Mowat‐Wilson” syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies‐mental retardation syndrome caused by mutations in the zinc finger homeo box 1B geneAmerican Journal of Medical Genetics, 2002
- Nonsense and Frameshift Mutations in ZFHX1B, Encoding Smad-Interacting Protein 1, Cause a Complex Developmental Disorder with a Great Variety of Clinical FeaturesAmerican Journal of Human Genetics, 2001
- Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline StructuresAmerican Journal of Human Genetics, 2001
- α4 integrin is expressed in a subset of cranial neural crest cells and in epicardial progenitor cells during early mouse developmentMechanisms of Development, 2000
- SOX10 mutations in patients with Waardenburg-Hirschsprung diseaseNature Genetics, 1998
- Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2Nature, 1996
- Expression of M‐twist during postimplantation development of the mouseDevelopmental Dynamics, 1995
- Dorsal differentiation of neural plate cells induced by BMP-mediated signals from epidermal ectodermCell, 1995
- A new family of mouse homeo box-containing genes: molecular structure, chromosomal location, and developmental expression of Hox-7.1.Genes & Development, 1989
- Expression of N-cadherin adhesion molecules associated with early morphogenetic events in chick developmentNature, 1986