Showing results 1 to 3 of 3
Title | Author(s) | Issue Date | |
---|---|---|---|
Patient-reported outcomes in a Chinese cohort of osteogenesis imperfecta unveil psycho-physical stratifications associated with clinical manifestations Journal:Orphanet Journal of Rare Diseases | 2022 | ||
Phenotypic spectrum and molecular basis in a Chinese cohort of osteogenesis imperfecta with mutations in type I collagen Journal:Frontiers in Genetics, section Genetics of Common and Rare Diseases | 2022 | ||
Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patients Journal:Orphanet Journal of Rare Diseases | 20-Sep-2023 |