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...

Descripción completa

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

Ejemplares similares

Ejemplares similares