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:
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- 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