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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 期刊论文
Bone, 2008, 卷号: Vol.42 No.4, 页码: 631-643
作者:  Liangjun Yin;  Xiaolan Du;  Cuiling Li;  Xiaoling Xu;  Zhi Chen
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