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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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| Publicat a: | J Clin Exp Dent |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medicina Oral S.L.
2016
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| Matèries: | |
| Accés en línia: | 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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