Published in

Elsevier, Genetics in Medicine, 4(22), p. 701-708, 2020

DOI: 10.1038/s41436-019-0729-1

Links

Tools

Export citation

Search in Google Scholar

Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

Full text: Download

Green circle
Preprint: archiving allowed
Red circle
Postprint: archiving forbidden
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO