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Article

[Genetic origin of non-syndromic cleft lip and palate. TWIST, a candidate gene? Research protocol].

L' Orthodontie francaise - 1 Dec 2007

Bacon William, Tschill Pascal, Grollemund Bruno, Matern Olivier, Rinkenbach Renaud, Sauvage Paul, Kaufmann Isabelle, Bousquet Pascal, Brandt Christian, Perrin-Schmitt Fabienne

Abstract excerpt

Non syndromic cleft lip and palate (CLP) is the most frequent human malformation. CLP is of complex inheritance and at least twenty contributing chromosomal regions have been identified by linkage studies. On the other hand, mutations in several genes such as TWIST and FGFR2 result in syndromic c...

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Source

Identifiers

PMID: 18082115
DOI: 10.1051/orthodfr:2007028

Genes

FGFR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18082115-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Genetic origin of non-syndromic cleft lip and palate. TWIST, a candidate gene? Research protocol].PMID 18082115Read ↗

[Genetics of craniofacial malformations].Semantic proximity Read ↗

Mutations of the TWIST gene in the Saethre-Chotzen syndrome.Semantic proximity Read ↗

Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants.Semantic proximity Read ↗

Clinical findings in four Brazilian families affected by Saethre-Chotzen syndrome without TWIST mutations.Semantic proximity Read ↗

Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locus.Semantic proximity Read ↗

[Clinical and molecular genetic observations on families with cherubism over three generations].Semantic proximity Read ↗

Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome.Semantic proximity Read ↗

Deletion involving the TWIST locus and the HOXA cluster: a contiguous gene syndrome on 7p?Semantic proximity Read ↗

Do Craniosynostosis syndrome phenotypes with both FGFR2 and TWIST mutations have a worse clinical outcome?Semantic proximity Read ↗

Mutations in the human TWIST gene.Semantic proximity Read ↗

Clinical and genetic analysis of patients with Saethre-Chotzen syndrome.Semantic proximity Read ↗

Evidence of an involvement of TFAP2A gene in non-syndromic cleft lip with or without cleft palate: an Italian study.Semantic proximity Read ↗

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