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Gorlin syndrome presenting with a unilateral ovarian fibroma in a 22-year-old woman: a case report
INTRODUCTION: Nevoid basal cell carcinoma syndrome, or Gorlin syndrome, is an inherited disorder characterized by malignancies of the skin and other organs, skeletal abnormalities, and congenital malformations. The syndrome follows an autosomal dominant inheritance pattern with a gene mutation local...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3423051/ https://ncbi.nlm.nih.gov/pubmed/22691621 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-6-148 |
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