Long-term follow-up of ETV6-RUNX1 ALL reveals that NCI risk, rather than secondary genetic abnormalities, is the key risk factor. (2013)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/leu.2013.136

PubMed Identifier: 23636228

Publication URI: http://europepmc.org/abstract/MED/23636228

Type: Journal Article/Review

Volume: 27

Parent Publication: Leukemia

Issue: 11

ISSN: 0887-6924