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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

Developmental BiologyBone Morphogenic ProteinBone RepairOsteoarthritisPathologyOsteogenesisOsteoporosisMedicineOrthopaedic SurgeryHuman Apert SyndromePro253arg MutationSkeleton Malformation