← Evidence map

ArticleJCO precision oncology2019

Expanded analysis of secondary germline findings from matched tumor/normal sequencing identifies additional clinically significant mutations.

E Ileana Dumbrava et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

8 papers cite it

2019
2020
2021
2022
2023
2024
this papercites it

The trial

Full record →Abstract, authors, funding and every citing paper · PMID 31517177