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- W2801334414 abstract "Orofacial clefts (OFC) are complex genetic traits that are often classified as syndromic or non-syndromic clefts. To date, over 500 types of syndromic clefts have been identified and listed in the Online Mendelian Inheritance in Man (OMIM) database (www.omim.org), and the underlying genetic factors for many of these have been identified. Van der Woude syndrome (VWS) (OMIM: 119300) is a dominantly inherited developmental disorder with high penetrance (96.7%) but variable expression.1 VWS is characterized by pits and/or sinuses of the lower lip, cleft lip (CL), cleft lip and palate (CLP), or cleft palate only." @default.
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- W2801334414 date "2019-04-01" @default.
- W2801334414 modified "2023-10-14" @default.
- W2801334414 title "Novel mutations of IRF6 gene in Taiwanese Van der Woude syndrome patients" @default.
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- W2801334414 doi "https://doi.org/10.1016/j.pedneo.2018.04.008" @default.
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