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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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| Publicado en: | Dentomaxillofac Radiol |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
The British Institute of Radiology.
2016
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| Materias: | |
| Acceso en línea: | 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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