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Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine ?1(I) 901 substitution in a type-I collagen gene

Bone DiseaseDevelopmental BiologyBone Morphogenic ProteinGeneticsOsteoarthritisOsteogenesisType-i Collagen GeneOsteoporosisIntrafamilial VariabilityMedicineOrthopaedic SurgeryOsteocalcinConnective Tissue Disease