Associated Papers
Causal Variations at IRF6 Gene Identified in Van der Woude Syndrome Pedigrees.
Yang CW et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2024
36866619 (PubMed )
Supplement: sj-docx-1-cpc-10.1177_10556656231157575.docx
Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndrome.
Alade AA et al.
Molecular Genetics & Genomic Medicine, 2020
32558391 (PubMed )
Supplement: MGG3-8-e1355-s001.xlsx › Sheet2
Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome.
Yeetong P et al.
American Journal of Medical Genetics. Part A, 2009
Select a paper to view details