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Cleidocranial Dysplasia with Autosomal Dominant Inheritance Pattern
Cleidocranial dysplasia (CCD) is an autosomal dominant disease with a wide range of expression, characterized by clavicular hypoplasia, retarded cranial ossification, delayed bone and teeth development, supernumerary teeth, stomatognathic, craniofacial and skeletal abnormalities. This paper presents...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Medknow Publications & Media Pvt Ltd
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4145514/ https://ncbi.nlm.nih.gov/pubmed/25184084 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2141-9248.138042 |
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