FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome

The aim of the present study was to identify mutations in the fibroblast growth factor receptor 2 (FGFR2) gene in patients with Crouzon syndrome and characterize the associated clinical features. A total of two Chinese patients diagnosed with Crouzon syndrome underwent complete examinations, includi...

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Detalles Bibliográficos
Autores principales: Lin, Ying, Gao, Hongbin, Ai, Siming, Eswarakumar, Jacob V.P., Zhu, Yi, Chen, Chuan, Li, Tao, Liu, Bingqian, Jiang, Hongye, Liu, Yuhua, Li, Yonghao, Wu, Qingxiu, Li, Haichun, Liang, Xiaoling, Jin, Chenjin, Huang, Xinhua, Lu, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865782/
https://www.ncbi.nlm.nih.gov/pubmed/28901406
http://dx.doi.org/10.3892/mmr.2017.7397

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865782/
https://www.ncbi.nlm.nih.gov/pubmed/28901406
http://dx.doi.org/10.3892/mmr.2017.7397

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