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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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Detalhes bibliográficos
Publicado no:Neuro Oncol
Main Authors: Karschnia, P, Erson-Omay, E Z, Huttner, A J, Fulbright, R K, Günel, M, Baehring, J M
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
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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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