| 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 |