← Evidence map

ArticleNPJ genomic medicine2016

Development and validation of a whole-exome sequencing test for simultaneous detection of point mutations, indels and copy-number alterations for precision cancer care.

Hanna Rennert et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

48 papers cite it

2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 28781886