FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome-Reference-Cited by-同舟云学术

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

Published:2017-05 Issue:5 Volume:16 Page:5841-5846
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

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

Publisher

Spandidos Publications

Subject

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

Cited by 11 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. Ocular manifestations and treatment progress of Crouzon syndrome;International Ophthalmology;2024-09-05

2. Identification of Diagnostic Variants in FGFR2 and NPR2 Genes in a Chinese Family Affected by Crouzon Syndrome and Acromesomelic Dysplasia, Type Maroteaux;DNA and Cell Biology;2022-11-01

3. FGFR2 Mutation p.Cys342Arg Enhances Mitochondrial Metabolism-Mediated Osteogenesis via FGF/FGFR-AMPK-Erk1/2 Axis in Crouzon Syndrome;Cells;2022-10-05

4. Genética‌‌ de‌‌ las‌‌ fisuras‌‌ labiopalatinas‌‌:‌ una‌‌ visión‌ general‌‌ de‌‌ los‌‌ factores‌‌ de‌‌ riesgo‌‌ genéticos‌‌ y‌‌ ambientales;Revista Med;2022-08-01

5. Crouzon syndrome in a fraternal twin: A case report and review of the literature;World Journal of Clinical Cases;2022-06-06

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