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Frontiers | Functional Characterization of a Novel IRF6 Frameshift Mutation From a Van Der Woude Syndrome Family
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A rare case of familal van der woude syndrome Vallabhaneni K, Muktineni S, Avula SS, Korikani A - Int J Pedod Rehabil
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Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene | Journal of Medical Genetics
DBMCI - MDS Experts : the NEET MDS Experts - VAN-DER WOUDE SYNDROME • It is genetic condition with autosomal dominant inheritance which affects development of face. CLINICAL FEATURES • Lower lip
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Management of Lip Pits in Van der Woude Syndrome: A Clinical Classification With Difficulty Index - ScienceDirect
![Bilateral cleft of lip and palate in association with van der Woude... | Download Scientific Diagram Bilateral cleft of lip and palate in association with van der Woude... | Download Scientific Diagram](https://www.researchgate.net/publication/5248923/figure/fig6/AS:601669771485213@1520460660535/Bilateral-cleft-of-lip-and-palate-in-association-with-van-der-Woude-syndrome.png)