Recurrent genetic fusions redefine MLL germ line acute lymphoblastic leukemia in infants
Language English Country United States Media print
Document type Letter, Research Support, Non-U.S. Gov't
PubMed
33512459
DOI
10.1182/blood.2020009032
PII: S0006-4971(20)86028-5
Knihovny.cz E-resources
- MeSH
- Oncogene Proteins, Fusion genetics MeSH
- Gene Rearrangement MeSH
- Histone-Lysine N-Methyltransferase genetics MeSH
- Infant MeSH
- Humans MeSH
- Oncogene Fusion * MeSH
- Precursor B-Cell Lymphoblastic Leukemia-Lymphoma genetics pathology therapy MeSH
- Myeloid-Lymphoid Leukemia Protein genetics MeSH
- Retrospective Studies MeSH
- Germ Cells pathology MeSH
- Check Tag
- Infant MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Letter MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Oncogene Proteins, Fusion MeSH
- Histone-Lysine N-Methyltransferase MeSH
- KMT2A protein, human MeSH Browser
- Myeloid-Lymphoid Leukemia Protein MeSH
Bicocca Bioinformatics Biostatistics and Bioimaging Centre School of Medicine and Surgery and
Central European Institute of Technology Brno Czech Republic
Department of Pediatric Onco Hematology Regina Margherita Children's Hospital Turin Italy
Genetics School of Medicine and Surgery University of Milan Bicocca Monza Italy
Pediatric Hematology Oncology Fondazione IRCCS Policlinico San Matteo Pavia Italy
Pediatrics University of Milan Bicocca Fondazione MBBM San Gerardo Hospital Monza Italy; and
Woman and Child Health Department OncoHematology Laboratory University of Padua Padua Italy
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