Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Coding region of IRF6 gene may not be causal for Van der Woude syndrome in cases from India.

The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association - 1 Sept 2009

Ali Akhtar, Singh Subodh Kumar, Raman Rajiva

Abstract excerpt

OBJECTIVE: Evaluation of the IRF6 gene in Van der Woude syndrome cases from an Indian population. SUBJECTS: Nine affected and four unaffected individuals from seven families with Van der Woude syndrome as well as five normal controls (with no history of Van der Woude or any other congenital malfo...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to 3' Untranslated Regions
Share to Adenine
Share to Cleft Lip

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cleft Palate

Share to Cytosine

Share to Guanine

Share to Interferon Regulatory Factors

Share to Thymine

Source

Identifiers

PMID: 19929101
DOI: 10.1597/08-202.1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19929101-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Coding region of IRF6 gene may not be causal for Van der Woude syndrome in cases from India.PMID 19929101Read ↗

Identification of IRF6 gene variants in three families with Van der Woude syndrome.Semantic proximity Read ↗

Non‐random distribution of deleterious mutations in the DNA and protein‐binding domains of IRF6 are associated with Van Der Woude syndromeSemantic proximity Read ↗

Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family.Semantic proximity Read ↗

Novel mutations in the IRF6 gene in Brazilian families with Van der Woude syndrome.Semantic proximity Read ↗

Identification of novel mutations of IRF6 gene in Chinese families with Van der Woude syndrome.Semantic proximity Read ↗

Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.Semantic proximity Read ↗

Novel mutations in the IRF6 gene for Van der Woude syndrome.Semantic proximity Read ↗

[Genetic analysis of a family of Van der Woude syndrome].Semantic proximity Read ↗

A novel mutation of the IRF6 gene in an Italian family with Van der Woude syndrome.Semantic proximity Read ↗

Causal Variations at IRF6 Gene Identified in Van der Woude Syndrome Pedigrees.Semantic proximity Read ↗

Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.Semantic proximity Read ↗

[Analysis of a Chinese pedigree affected with van der Woude syndrome due to variant of IRF6 gene].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.