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Orthodontic and surgical management of cleidocranial dysplasia
Published Web Location
http://europepmc.org/articles/PMC3822065?pdf=renderNo data is associated with this publication.
Abstract
Cleidocranial dysplasia (CCD), an autosomal dominant disorder with a prevalence of 1 in 1,000,000 individuals, is mainly caused by mutations in Runx2, a gene required for osteoblastic differentiation. It is generally characterized by hypoplastic clavicles,
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