A 13-year-old caucasian boy with cleidocranial dysplasia: a case report
<p>Abstract</p> <p>Background</p> <p>Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal disorder. The disorder is caused by heterozygosity of mutations in human <it>RUNX2</it>, which is present on the short arm of chromosome 6p21&...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2013-01-01
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| Series: | BMC Research Notes |
| Subjects: | |
| Online Access: | http://www.biomedcentral.com/1756-0500/6/6 |