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RUNX2 analysis of Danish cleidocranial dysplasia families

โœ Scribed by L Hansen; AK Riis; A Silahtaroglu; H Hove; E Lauridsen; H Eiberg; S Kreiborg


Book ID
110889065
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
682 KB
Volume
79
Category
Article
ISSN
0009-9163

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## Communicated by Gregg Semenza Cleidocranial dysplasia (CCD) is a autosomal dominant disorder characterized by skeletal anomalies such as patent fontanels, late closure of cranial sutures with Wormian bones, late erupting secondary dentition, rudimentary clavicles, and short stature. The locus f