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Treacher Collins综合征的致病基因和临床治疗策略
Treacher Collins syndrome is a congenital craniofacial malformation with autosomal dominant inheritance as the main genetic pattern. In this condition, the biosynthesis of ribosomes in neural crest cells and neuroepithelial cells is blocked and the number of neural crest cells that migrate to the cr...
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| Yayımlandı: | Hua Xi Kou Qiang Yi Xue Za Zhi |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
华西口腔医学杂志编辑部
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7030091/ https://ncbi.nlm.nih.gov/pubmed/31218872 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7518/hxkq.2019.03.020 |
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