C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients

The current study was performed with aim to investigate the fibroblast growth factor receptor 2 (FGFR2) gene in two Chinese families with two different forms of syndromic craniosynostosis, and to characterize their associated clinical features. Two families underwent complete ophthalmic examinations...

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Detalles Bibliográficos
Autores principales: Lin, Ying, Gao, Hongbin, Ai, Siming, Eswarakumar, Jacob V.P., Chen, Chuan, Zhu, Yi, Li, Tao, Liu, Bingqian, Liu, Xialin, Luo, Lixia, Jiang, Hongye, Li, Yonghao, 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/PMC5647065/
https://www.ncbi.nlm.nih.gov/pubmed/28849010
http://dx.doi.org/10.3892/mmr.2017.7248

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647065/
https://www.ncbi.nlm.nih.gov/pubmed/28849010
http://dx.doi.org/10.3892/mmr.2017.7248

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