Mutation screening in theIRF6-gene in patients with apparently nonsyndromic orofacial clefts and a positive family history suggestive of autosomal-dominant inheritance-Reference-Cited by-同舟云学术

Mutation screening in theIRF6-gene in patients with apparently nonsyndromic orofacial clefts and a positive family history suggestive of autosomal-dominant inheritance

Published:2008 Issue:6 Volume:146A Page:787-790
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Birnbaum Stefanie,Reutter Heiko,Lauster Carola,Scheer Martin,Schmidt Gül,Saffar Mitra,Martini Markus,Hemprich Alexander,Henschke Henning,Kramer Franz-Josef,Mangold Elisabeth

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Variation in IRF6 contributes to nonsyndromic cleft lip and palate

2. Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population

3. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

4. . 2002. Epidemiology of oral clefts: An international perspective. In: editor. Cleft lip and palate: From origin to treatment. Oxford: Oxford University Press. p 127–144.

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2. Case report and functional verification of a novel mutation in the interferon regulatory transcription factor 6 gene in a family with orofacial clefts;American Journal of Translational Research;2024

3. Novel IRF6 variant in orofacial cleft patients from Durban, South Africa;Molecular Genetics & Genomic Medicine;2023-02-21

4. Screening of IRF6 Variants in Patients Subjected to Genetic Association Studies for Nonsyndromic Cleft Lip/Palate;The Cleft Palate-Craniofacial Journal;2020-12-17

5. A Novel IRF6 Variant Detected in a Family With Nonsyndromic Cleft Lip and Palate by Whole Exome Sequencing;Journal of Craniofacial Surgery;2020-10-29