Nalaganje...
A 13-year-old caucasian boy with cleidocranial dysplasia: a case report
BACKGROUND: Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal disorder. The disorder is caused by heterozygosity of mutations in human RUNX2, which is present on the short arm of chromosome 6p21. The incidence of CCD is one per million births. CCD appears spontaneously w...
Shranjeno v:
| Main Authors: | , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2013
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3551643/ https://ncbi.nlm.nih.gov/pubmed/23289840 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-0500-6-6 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|