Genetic Variants in IRF6 and the Risk of Facial Clefts: Single-Marker and Haplotype-Based Analyses in a Population-Based Case-Control Study of Facial Clefts in Norway

Mutations in the gene encoding interferon regulatory factor 6 (IRF6) underlie a common form of syndromic clefting known as Van der Woude syndrome. Lip pits and missing teeth are the only additional features distinguishing the syndrome from isolated clefts. Van der Woude syndrome, therefore, provides...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Jugessur, Astanand, Rahimov, Fedik, Lie, Rolv T., Wilcox, Allen J., Gjessing, Håkon K., Nilsen, Roy M., Nguyen, Truc Trung, Murray, Jeffrey C.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2008
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2680842/
https://ncbi.nlm.nih.gov/pubmed/18278815
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.20314
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