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Xp11.2 translocation renal cell carcinoma with multiple bone metastases: A case report
Xp11.2 translocation/transcription factor enhancer 3 (TFE3) fusion gene associated with renal cell carcinoma (Xp11.2 translocation RCC) is rare and occurs predominantly in children and adolescents. The current study reports the case of a 14-year-old male with Xp11.2 translocation RCC, who presented...
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| Publicat a: | Oncol Lett |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
D.A. Spandidos
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4774413/ https://ncbi.nlm.nih.gov/pubmed/26998154 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2016.4211 |
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