C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients-Reference-Cited by-同舟云学术

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

Published:2017-08-14 Issue:4 Volume:16 Page:5333-5337
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

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

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Phenotypic variability of syndromic craniosynostosis caused by c.833G > T in FGFR2 : Clinical and genetic evaluation of eight patients from a five‐generation family;Molecular Genetics & Genomic Medicine;2022-03-02

2. Clinical assessment and FGFR2 mutation analysis in a Chinese family with Crouzon syndrome;Medicine;2021-03-12

3. Targeted next‑generation sequencing identifies two novel COL2A1 gene mutations in Stickler syndrome with bilateral retinal detachment;International Journal of Molecular Medicine;2018-07-04

4. Genetic variations in Bestrophin-1 and associated clinical findings in two Chinese patients with juvenile-onset and adult-onset best vitelliform macular dystrophy;MOL MED REP;2018

5. Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy;International Journal of Molecular Medicine;2017-12-05

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