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FGFR2 molecular analysis and related clinical findings in one Chinese family with Crouzon Syndrome

PURPOSE: The purposed of this study was to investigate the fibroblast growth factor receptor 2 (FGFR2) gene in one Chinese family with Crouzon syndrome and to characterize the related clinical features. METHODS: One family underwent complete ophthalmic examinations, and two patients were diagnosed w...

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Detalhes bibliográficos
Main Authors: Lin, Ying, Liang, Xuanwei, Ai, Siming, Chen, Chuan, Liu, Xialin, Luo, Lixia, Ye, Shaobi, Li, Baoxin, Liu, Yizhi, Yang, Huasheng
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3283207/
https://ncbi.nlm.nih.gov/pubmed/22355256
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