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Article

Association of MSX1 c.*6C > T Variant with Nonsyndromic Cleft Lip With or Without Cleft Palate in Turkish Patients.

Genetic testing and molecular biomarkers - 1 Jul 2016

Aslar Oner Deniz, Tastan Hakki

Abstract excerpt

OBJECTIVE: Nonsyndromic cleft lip with or without cleft palate (nsCL/P) is among the most common birth defects, with a birth prevalence of 1/1000 in Caucasians. MSX1 (muscle segment homeobox gene 1) is a strong candidate gene for nsCL/P. The aim of this study was to investigate the association between MSX1 variants and nsCL/P in Turkish patients. PATIENTS AND METHODS: Our study included 80 patients with nsCL/P...

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Source

Identifiers

PMID: 27228008
DOI: 10.1089/gtmb.2015.0341

Genes

MSX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Association of MSX1 c.*6C > T Variant with Nonsyndromic Cleft Lip With or Without Cleft Palate in Turkish Patients.PMID 27228008Read ↗

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