Human Genome Epidemiology Literature Finder
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Query Trace: Retinal Detachment and FGFR2[original query] |
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C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients. Molecular medicine reports 2017 Aug . 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 L |
- Page last reviewed:Feb 1, 2024
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