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Cleidocranial dysplasia: A report of two cases with brief review
Cleidocranial dysplasia (CCD) is a genetic disorder primarily causing dysplasia of bones and teeth with autosomal dominant inheritance pattern. Affected individuals presented with several skeletal and dental abnormalities mainly hypoplasia of clavicles, open fontanelles, short stature, retention of...
保存先:
| 出版年: | Intractable Rare Dis Res |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4869578/ https://ncbi.nlm.nih.gov/pubmed/27195196 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2016.01022 |
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