Craniometaphyseal dysplasia: the need for a natural history of disease study
Craniometaphyseal dysplasia (CMD) is a rare genetic skeletal disorder, whose biological understanding is not very well known. The disease manifests itself through bony hypertrophy of the skull base, craniofacial bones, and abnormal morphology of the long bones, present in the carrier of the disease....
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| Language: | en_US |
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2016
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| Online Access: | https://hdl.handle.net/2144/16816 |