Revisiting coexisting chromosomal abnormalities in NPM1-mutated AML in light of the revised ELN 2022 classification
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
36327154
DOI
10.1182/blood.2022018582
PII: S0006-4971(22)07952-6
Knihovny.cz E-resources
- MeSH
- Leukemia, Myeloid, Acute * genetics MeSH
- Chromosome Aberrations * MeSH
- Nuclear Proteins genetics MeSH
- Humans MeSH
- Mutation MeSH
- Prognosis MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Nuclear Proteins MeSH
Centre Hospitalier Universitaire de Toulouse Toulouse France
Centro de Investigación Biomédica en Red de Cáncer Madrid Spain
Department of Biosystems Science and Engineering ETH Zurich Basel Switzerland
Department of Medicine A Münster University Hospital Münster Germany
Dresden University Hospital Technical University Dresden Dresden Germany
Faculty of Medicine Masaryk University Brno Czech Republic
Hospital Universitari i Politècnic La Fe Valencia Spain
Paris Diderot University Paris France
The University of Texas MD Anderson Cancer Center Houston TX
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