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Gorlin-Goltz syndrome: incidental finding on routine ct scan following car accident
INTRODUCTION: Gorlin-Goltz syndrome is a rare hereditary disease. Pathogenesis of the syndrome is attributed to abnormalities in the long arm of chromosome 9 (q22.3-q31) and loss or mutations of human patched gene (PTCH1 gene). Multiple basal cell carcinomas (BCCs), odontogenic keratocysts, skeletal...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2803884/ https://ncbi.nlm.nih.gov/pubmed/20062724 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1757-1626-2-9087 |
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