Literature DB >> 1942786

[Crouzon syndrome (Mc K 12350)].

B Mitulla1, G K Hinkel, P Lorenz.   

Abstract

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Mesh：

Year:  1991        PMID： 1942786

Source DB:  PubMed          Journal:  Kinderarztl Prax        ISSN： 0023-1495


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  4 in total

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

Authors:  Ying Lin; Hongbin Gao; Siming Ai; Jacob V P Eswarakumar; Chuan Chen; Yi Zhu; Tao Li; Bingqian Liu; Xialin Liu; Lixia Luo; Hongye Jiang; Yonghao Li; Xiaoling Liang; Chenjin Jin; Xinhua Huang; Lin Lu
Journal:  Mol Med Rep       Date:  2017-08-14       Impact factor: 2.952

2.  Detection of G338R FGFR2 mutation in a Vietnamese patient with Crouzon syndrome.

Authors:  Anh Lan Thi Luong; Thuong Thi Ho; Ha Hoang; Trung Quang Nguyen; Tu Cam Ho; Phan Duc Tran; Thuy Thi Hoang; Nam Trung Nguyen; Hoang Ha Chu
Journal:  Biomed Rep       Date:  2019-01-03

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

Authors:  Yidi Wang; Yue Liu; Haotian Chen; Xiaojing Liu; Yi Zhang; Yixiang Wang; Yan Gu
Journal:  Cells       Date:  2022-10-05       Impact factor: 7.666

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

Authors:  Ying Lin; Hongbin Gao; Siming Ai; Jacob V P Eswarakumar; Yi Zhu; Chuan Chen; Tao Li; Bingqian Liu; Hongye Jiang; Yuhua Liu; Yonghao Li; Qingxiu Wu; Haichun Li; Xiaoling Liang; Chenjin Jin; Xinhua Huang; Lin Lu
Journal:  Mol Med Rep       Date:  2017-08-29       Impact factor: 2.952
  4 in total

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