A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis (Q46777447)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis |
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A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis (English)
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Liangjun Yin
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Xiaolan Du
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Cuiling Li
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Xiaoling Xu
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Zhi Chen
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Nan Su
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Ling Zhao
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Huabing Qi
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Fubing Li
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Jing Xue
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Jing Yang
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Min Jin
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Chuxia Deng
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Lin Chen
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31 January 2008
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42
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631-643
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4
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