Laddar...
Dysregulation of Chondrogenesis in Human Cleidocranial Dysplasia
Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal dysplasia caused by heterozygosity of mutations in human RUNX2. The disorder is characterized by delayed closure of the fontanel and hypoplastic clavicles that result from defective intramembranous ossification. However, additional feat...
Sparad:
| Huvudupphovsmän: | , , , , , , |
|---|---|
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
The American Society of Human Genetics
2005
|
| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1224532/ https://ncbi.nlm.nih.gov/pubmed/15952089 |
| Taggar: |
Lägg till en tagg
Inga taggar, Lägg till första taggen!
|