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FGFR2 mutation in a Chinese family with unusual Crouzon syndrome
AIM: To describe the clinical characteristics with genetic lesions in a Chinese family with Crouzon syndrome. METHODS: All five patients from this family were included and received comprehensive ophthalmic and systemic examinations. Direct sequencing of the FGFR2 gene was employed for mutation ident...
Shranjeno v:
| izdano v: | Int J Ophthalmol |
|---|---|
| Main Authors: | , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
International Journal of Ophthalmology Press
2016
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5075653/ https://ncbi.nlm.nih.gov/pubmed/27803855 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18240/ijo.2016.10.06 |
| Oznake: |
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