PATH-50. ROUTINE MOLECULAR DIAGNOSIS OF GLIOMA PATIENTS USING A GLIOMA-SPECIFIC NGS PANEL

AIM: The 2016 WHO classification requires molecular diagnosis in routine glioma diagnostics. However, analysis of key driver gene mutations and chromosome 1p/19q co-deletions cannot be performed in a single platform. In this study, we evaluated the feasibility of a glioma-specific NGS panel for mole...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:Neuro Oncol
Main Authors: Yoshimoto, Koji, Higa, Nayuta, Yonezawa, Hajime, Uchida, Hiroyuki, Akahane, Toshiaki, Tanimoto, Akihide
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2019
Teme:
Molecular Pathology and Classification - Adult and Pediatric
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6847017/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noz175.646
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki