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Article

MSX1 gene polymorphisms in Mexican patients with non-syndromic cleft lip/palate.

International journal of pediatric otorhinolaryngology - 1 Nov 2016

Ibarra-Arce Aurora, Albavera-Giles Tania, Zavaleta-Villa Beatriz, Ortiz de Zárate-Alarcón Gabriela, Flores-Peña Laura, Sierra-Romero María Del Carmen, Romero-Valdovinos Mirza, Olivo-Díaz Angélica

Abstract excerpt

OBJECTIVE: Non-syndromic cleft lip/palate malformation (CL/P) is one of the most common birth defects in humans and has a complex etiology involving genetic and environmental factors. Mutations in the MSX1 gene are critical during craniofacial development. The purpose of this study was to investigate the contribution of MSX1 gene polymorphisms to the risk of developing CL/P in a sample of Mexican patients....

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Source

Identifiers

PMID: 27729116
DOI: 10.1016/j.ijporl.2016.09.008

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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