Multigene testing for hereditary cancer: When, why, and how

8Citations
Citations of this article
24Readers
Mendeley users who have this article in their library.

Abstract

Multigene testing is a complicated area, with advantages and disadvantages of testing for hereditary cancer syndromes. Currently, NCCN does not endorse routing multiplex testing outside of a research setting, and/or intensive genetic counseling regarding risks and benefits. The 2017 NCCN Clinical Practice Guidelines in Oncology for Genetic/Familial High-Risk Assessment: Breast and Ovarian and Colorectal provide suggestions for mutation carriers identified by panel tests.

Cite

CITATION STYLE

APA

Offit, K. (2017). Multigene testing for hereditary cancer: When, why, and how. In JNCCN Journal of the National Comprehensive Cancer Network (Vol. 15, pp. 741–743). Harborside Press. https://doi.org/10.6004/jnccn.2017.0089

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free