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Gorlin syndrome and bilateral ovarian fibroma
INTRODUCTION: Gorlin syndrome (GS), also known as nevoid basal cell carcinoma syndrome (NBCCS), is a rare hereditary, autosomal dominant disease that affects various systems. Its prevalence is estimated at 1/57,000 to 1/256,000 of the population. It is characterized by basal cell carcinomas, multipl...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3397296/ https://ncbi.nlm.nih.gov/pubmed/22771908 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijscr.2012.05.015 |
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