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Synchronous Presentation of Rare Brain Tumors in Von Hippel–Lindau Syndrome
Von Hippel–Lindau (VHL) disease is a heritable cancer syndrome in which benign and malignant tumors and/or cysts develop throughout the central nervous system (CNS) and visceral organs. The disease results from mutations in the VHL tumor suppressor gene located on chromosome 3 (3p25-26). A majority...
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| 發表在: | Diagnostics (Basel) |
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| Main Authors: | , , , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
MDPI
2021
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8228671/ https://ncbi.nlm.nih.gov/pubmed/34072835 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diagnostics11061005 |
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