DNA methylation differences in monozygotic twins with Van der Woude syndrome

INTRODUCTION: Van 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 phen...

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Detalles Bibliográficos
Autores principales: Petrin, A. L., Zeng, E., Thomas, M. A., Moretti-Ferreira, D., Marazita, M. L., Xie, X. J., Murray, J. C., Moreno-Uribe, L. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019782/
https://www.ncbi.nlm.nih.gov/pubmed/36936396
http://dx.doi.org/10.3389/fdmed.2023.1120948

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019782/
https://www.ncbi.nlm.nih.gov/pubmed/36936396
http://dx.doi.org/10.3389/fdmed.2023.1120948

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