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Journal Article
Journal Article
Journal Article
Molecular medicine reports, 09/2016, Volume 14, Issue 3, p. 2710
Camurati-Engelmann disease (CED; MIM 131300), or progressive diaphyseal dysplasia, is a rare autosomal dominant bone disease, which is caused by mutations in... 
Bone Density | Genetic Testing | Humans | Camurati-Engelmann Syndrome - genetics | Transforming Growth Factor beta1 - genetics | Camurati-Engelmann Syndrome - blood | Exophthalmos - diagnosis | Young Adult | Multimodal Imaging | Phenotype | DNA Mutational Analysis | Camurati-Engelmann Syndrome - diagnosis | Biomarkers | Female | Mutation
Journal Article
Journal Article