| Literature DB >> 30327352 |
.
Abstract
The FDA granted marketing authorization to the first-ever next-generation sequencing assay for detecting minimal residual disease in patients with acute lymphoblastic leukemia or multiple myeloma. ©2018 American Association for Cancer Research.Entities:
Year: 2018 PMID: 30327352 DOI: 10.1158/2159-8290.CD-NB2018-136
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397