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Osteogenesis imperfecta
Osteogenesis imperfecta is a phenotypically and molecularly heterogeneous group of inherited connective tissue disorders that share similar skeletal abnormalities causing bone fragility and deformity. Previously, the disorder was thought to be an autosomal dominant bone dysplasia caused by defects i...
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| Udgivet i: | Lancet |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7384887/ https://ncbi.nlm.nih.gov/pubmed/26542481 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S0140-6736(15)00728-X |
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