?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 gene
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference21 articles.
1. Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease
2. XSIP1, a Member of Two-Handed Zinc Finger Proteins, Induced Anterior Neural Markers in Xenopus laevis Animal Cap
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