A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude Syndrome
Copyright policy ) Manuel González-García; Joaquin Fernandez-Toral; Lorena Miñones-Suárez; Isabel Llano-Rivas; Alberto Mas-Vidal;
A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude Syndrome
Abstract: This report describes a novel missense mutation in the interferon regulation factor 6 (IRF6) gene associated to facial asymmetry. This new feature widens the phenotype spectrum of Van der Woude syndrome (VWS).
Family Health, Male, Cysts, Cleft Lip, Mutation, Missense, Twins, Infant, Lip, Pedigree, Cleft Palate, Phenotype, Interferon Regulatory Factors, Humans, Abnormalities, Multiple
Family Health, Male, Cysts, Cleft Lip, Mutation, Missense, Twins, Infant, Lip, Pedigree, Cleft Palate, Phenotype, Interferon Regulatory Factors, Humans, Abnormalities, Multiple
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
Citations provided by BIP!popularityPopularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
Popularity provided by BIP! 8
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