Cleidocranial Dysplasia
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Genetics and Molecular Biology - RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia
scielo.br — “Genetics and Molecular Biology - RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia” View full resource at scielo.br
Most Recently Shared on May 21, 2011 at 11:05 am By:
RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia: Cleidocranial dysplasia (CCD) is an autosoma... http://bit.ly/iqPD1y
Journal of Medical Case Reports | Abstract | Cleidocranial dysplasia presenting with retained deciduous teeth in a 15-year-old girl: a case report
jmedicalcasereports.com — “Cleidocranial dysplasia is a rare congenital defect of autosomal dominant inheritance caused by mutations in the Cbfa1 gene, also called Runx2, located on the short arm of chromosome 6. It primarily affects bones which undergo intramembranous ossification. This condition is of clinical significance to dentistry due to the involvement of the facial bones, altered eruption patterns and multiple supernumerary teeth.” View full resource at jmedicalcasereports.com
Most Recently Shared on January 20, 2012 at 4:43 pm By:
JMedCaseReports Medical Journal
Latest from #JMCR http://t.co/cSQVVGyt Cleidocranial dysplasia presenting with retained deciduous teeth
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