DNA methylation differences in monozygotic twins with Van der Woude syndrome

IntroductionVan der Woude syndrome (VWS) is an autosomal dominant disorder responsible for 2% of all syndromic orofacial clefts (OFCs), with IRF6 being the primary causal gene (70%). Cases may present with lip pits and either cleft lip, cleft lip with cleft palate, or cleft palate, with marked pheno...

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Main Authors: A. L. Petrin (Author), E. Zeng (Author), M. A. Thomas (Author), D. Moretti-Ferreira (Author), M. L. Marazita (Author), X. J. Xie (Author), J. C. Murray (Author), L. M. Moreno-Uribe (Author)
Format: Book
Published: Frontiers Media S.A., 2023-02-01T00:00:00Z.
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