论文信息 - 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 Bone Formation - 字舞流文

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 Bone Formation

Bo Zhang | Bo Zhang | Shichang Zhang | Li Zhang | T. Weng | Lianyang Zhang | Peng-zhi Chen | Shijin Sun | Ming-tao Chang | Yang Li