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pro vyhledávání: '"Gerry Mc Manus"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-16 (2023)
Abstract Background Osteogenesis imperfecta (OI) is a rare, connective tissue disorder characterised by bone fragility, resulting in recurrent fractures and skeletal deformities. Extra-skeletal manifestations include dentinogenesis imperfecta, hearin
Externí odkaz:
https://doaj.org/article/a7a97ceb658b4e2b8995470efa861ae7
