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- W2236091708 startingPage "20150119" @default.
- W2236091708 abstract "Frank–ter Haar syndrome is a genetic disease that is transmitted by autosomal recessive pattern with characteristic features such as megalocornea or glaucoma, a prominent coccyx, heart defects, developmental delays, brachycephaly, a wide anterior fontanel, finger flexion deformities, full cheeks and micrognathia. Dentomaxillofacial features of this syndrome are not well documented in the literature. We present of a 21-year-old male with Frank–ter Haar syndrome and some features that may be linked with this syndrome not reported before in the literature." @default.
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- W2236091708 date "2016-02-01" @default.
- W2236091708 modified "2023-09-26" @default.
- W2236091708 title "Frank–ter Haar syndrome—additional findings?" @default.
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- W2236091708 doi "https://doi.org/10.1259/dmfr.20150119" @default.
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