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Mutational Analysis of TCOF1, GSC, and HOXA2 in Patients With Treacher Collins Syndrome
Treacher Collins syndrome is an autosomal dominant craniofacial malformation mainly caused by mutations in the TCOF1 gene. Few cases have been observed in the Chinese population. Herein, the authors report the mutational analysis of TCOF1, GSC, and HOXA2 to determine the mutational features of the 3...
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| Publicado no: | J Craniofac Surg |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Lippincott Williams & Wilkins
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5023764/ https://ncbi.nlm.nih.gov/pubmed/27526242 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/SCS.0000000000002934 |
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