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P04.60 Genomic profile of tumorigenesis in a patient with Turcot syndrome
BACKGROUND: Turcot syndrome (TS) represents a rare hereditary phenotype of mismatch repair (MMR) deficiency and is characterised by familial clustering of primary brain tumors in combination with abdominal tumors. MMR-deficient tumors in the setting of TS exhibit a characteristic molecular pattern:...
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| Publicado no: | Neuro Oncol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6143975/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noy139.294 |
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