Found: 6
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Clinical features and molecular characterization of Chinese patients with FKBP10 variants.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 4, p. 1, doi. 10.1002/mgg3.2122
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- Publication type:
- Article
Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patients.
- Published in:
- Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02906-z
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- Publication type:
- Article
Patient-reported outcomes in a Chinese cohort of osteogenesis imperfecta unveil psycho-physical stratifications associated with clinical manifestations.
- Published in:
- 2022
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- Publication type:
- journal article
Retrospective analyses of clinical features in 28 Chinese patients with type V osteogenesis imperfecta: new perspectives in an old issue.
- Published in:
- Osteoporosis International, 2023, v. 34, n. 2, p. 369, doi. 10.1007/s00198-022-06581-x
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- Publication type:
- Article
Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I Collagen.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.816078
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- Publication type:
- Article
Multi-omics analyses reveal aberrant differentiation trajectory with WNT1 loss-of-function in type XV osteogenesis imperfecta.
- Published in:
- Journal of Bone & Mineral Research, 2024, v. 39, n. 9, p. 1253, doi. 10.1093/jbmr/zjae123
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- Publication type:
- Article