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Article

Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate.

European journal of oral sciences - 1 Feb 2012

Mostowska Adrianna, Hozyasz Kamil K, Biedziak Barbara, Wojcicki Piotr, Lianeri Margarita, Jagodzinski Pawel P

Abstract excerpt

The wingless-type MMTV integration site family (Wnt) signalling pathway plays a crucial role in craniofacial development. Recently, nucleotide variants in WNT genes have been shown to be associated with oral congenital anomalies, including facial clefts. Therefore, in the current study we decided to assay the association of nucleotide variants in selected WNT genes with the risk of non-syndromic cleft lip with or...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22288914
DOI: 10.1111/j.1600-0722.2011.00938.x

Genes

NCL
WNT3
WNT11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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