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Multidisciplinary surgical management of Cowden syndrome: Report of a case
Cowden’s Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/200000 patients with an incomplete penetrance and variable expressivity, characterized by alterations in a tumor suppressor gene. A 14-year-old Caucasian male patient came to the attention of the authors co...
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| Yayımlandı: | J Clin Exp Dent |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Medicina Oral S.L.
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5045699/ https://ncbi.nlm.nih.gov/pubmed/27703620 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4317/jced.52919 |
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