Mutation screening in theIRF6‐gene in patients with apparently nonsyndromic orofacial clefts and a positive family history suggestive of autosomal‐dominant inheritance
- 4 February 2008
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 146A (6), 787-790
- https://doi.org/10.1002/ajmg.a.32219
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populationsGenetics in Medicine, 2007
- Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian populationEuropean Journal of Human Genetics, 2005
- Variation in IRF6 contributes to nonsyndromic cleft lip and palateAmerican Journal of Medical Genetics Part A, 2005
- Significant association between IRF6 820G->A and non-syndromic cleft lip with or without cleft palate in the Thai populationJournal of Medical Genetics, 2005
- Strong Evidence of Linkage Disequilibrium between Polymorphisms at the IRF6 Locus and Nonsyndromic Cleft Lip With or Without Cleft Palate, in an Italian PopulationAmerican Journal of Human Genetics, 2005
- Interferon Regulatory Factor 6 (IRF6) Gene Variants and the Risk of Isolated Cleft Lip or PalateNew England Journal of Medicine, 2004
- Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromesNature Genetics, 2002
- Epidemiology of Oral Clefts: An International PerspectivePublished by Oxford University Press (OUP) ,2002