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Allele Publication :

Type  Transmission Publication . Mgi Jnum  J:283626
Publication . Citation  Yin L, et al. (2008) A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis. Bone 42(4):631-43

1 Publication