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Broad Spectrum of Skeletal Malformation Complex in Patients with Cleidocranial Dysplasia Syndrome: Radiographic and Tomographic Study
PURPOSE: Cleidocranial dysplasia is an autosomal dominant disorder characterized by defective ossification of the intramembraneous ossification (primarily the clavicles, cranium, and pelvis), and it is caused by mutations in the RUNX2 gene that is responsible for osteoblast differentiation. Spine de...
Autores principales: | Al Kaissi, Ali, Ben Chehida, Farid, Kenis, Vladimir, Ganger, Rudolf, Radler, Christof, Hofstaetter, Jochen G., Klaushofer, Klaus, Grill, Franz |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762605/ https://www.ncbi.nlm.nih.gov/pubmed/24023524 http://dx.doi.org/10.4137/CMAMD.S11933 |
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