Literature DB >> 22028092

A novel fibroblast growth factor receptor 2 (FGFR2) mutation associated with a mild Crouzon syndrome.

Nicoletta Locuratolo1, M Baffico, M Baldi, V Parisi, F Micacchi, V Angelucci, M Rojas Beccaglia, C Pirro, Francesco Fattapposta.   

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Year:  2011        PMID： 22028092     DOI： 10.4449/aib.v149i3.1379

Source DB:  PubMed          Journal:  Arch Ital Biol        ISSN： 0003-9829            Impact factor:   1.000


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  2 in total

1.  FGFR2 molecular analysis and related clinical findings in one Chinese family with Crouzon syndrome.

Authors:  Ying Lin; Xuanwei Liang; Siming Ai; Chuan Chen; Xialin Liu; Lixia Luo; Shaobi Ye; Baoxin Li; Yizhi Liu; Huasheng Yang
Journal:  Mol Vis       Date:  2012-02-12       Impact factor: 2.367

2.  Ala344Pro mutation in the FGFR2 gene and related clinical findings in one Chinese family with Crouzon syndrome.

Authors:  Ying Lin; Siming Ai; Chuan Chen; Xialin Liu; Lixia Luo; Shaobi Ye; Xuanwei Liang; Yi Zhu; Huasheng Yang; Yizhi Liu
Journal:  Mol Vis       Date:  2012-05-15       Impact factor: 2.367
  2 in total

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