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Frank–ter Haar syndrome—additional findings?

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...

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Bibliografiska uppgifter
I publikationen:Dentomaxillofac Radiol
Huvudupphovsmän: Köse, Taha Emre, İşler, Cemil, Şenel, Ş Neslihan, Şitilci, Tolga, Özcan, İlknur, Aksakallı, Nihan
Materialtyp: Artigo
Språk:Inglês
Publicerad: The British Institute of Radiology. 2016
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5083953/
https://ncbi.nlm.nih.gov/pubmed/26582053
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1259/dmfr.20150119
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