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A Ser252Trp mutation in fibroblast growth factor receptor 2 (FGFR2) mimicking human Apert syndrome reveals an essential role for FGF signaling in the regulation of endochondral bon... by Peng Chen, Li Zhang, Tujun Weng, Shichang Zhang, Shijin Sun, Mingtao Chang, Yang Li, Bo Zhang, Lianyang Zhang
Published 2014-01-01
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