Nalaganje...

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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:Int J Ophthalmol
Main Authors: Li, Zi-Li, Chen, Xue, Zhuang, Wen-Juan, Zhao, Wei, Liu, Ya-Ni, Zhang, Fang-Xia, Ha, Ruo-Shui, Wu, Jin-Hua, Zhao, Chen, Sheng, Xun-Lun
Format: Artigo
Jezik:Inglês
Izdano: International Journal of Ophthalmology Press 2016
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: Označite
Brez oznak, prvi označite!