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Recurrent EGFR alterations in NTRK3 fusion negative congenital mesoblastic nephroma
OBJECTIVES: To identify oncogenic driver mutations in congenital mesoblastic nephroma (CMN) cases lacking ETV6-NTRK3 fusion and discuss their diagnostic value. DESIGN: The institutional pathology database was queried for cases with a morphologic diagnosis of CMN. Cases positive for ETV6 rearrangemen...
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| Publicado no: | Pract Lab Med |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7260589/ https://ncbi.nlm.nih.gov/pubmed/32490123 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.plabm.2020.e00164 |
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