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Article

MSX1 gene and nonsyndromic oral clefts in a Southern Brazilian population.

Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas - 1 Jul 2013

Souza L T, Kowalski T W, Collares M V M, Félix T M

Abstract excerpt

Nonsyndromic oral clefts (NSOC) are the most common craniofacial birth defects in humans. The etiology of NSOC is complex, involving both genetic and environmental factors. Several genes that play a role in cellular proliferation, differentiation, and apoptosis have been associated with clefting. For example, variations in the homeobox gene family member MSX1, including a CA repeat located within its single...

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Source

Open in PubMed Open full text

Identifiers

PMID: 23903689
DOI: 10.1590/1414-431X20133054
PMCID: PMC3859340

Genes

MSX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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