- Full text PDF available (0)
Journals and Conferences
OBJECTIVE To analyze the mutations of the RUNX2 gene in a family with cleidocranial dysplasia (CCD). METHODS The general health status of family members with CCD was investigated through propositus verification method. Oral specialized examination and radiological examination were performed. The peripheral venous blood of the proband and her parents and… (More)
Two cases of cleidocranial dysplasia(CCD) were reported and the characteristics of CCD were analyzed. The propositus verification method was used to family members for general health and oral specialized examination. All patients expressed developmental abnormality of crania, teeth and clavicle.