← Evidence map

ArticleAmerican journal of human genetics2003

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.

Tom Van de Putte et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

134 papers cite itlatest 60 shown

2003
…
2018
2019
2020
2021
2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 12522767