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Two rare cases of acute myeloid leukemia with t(8;16)(p11.2;p13.3) and 1q duplication: case presentation and literature review
BACKGROUND: Acute myeloid leukemia (AML) is a complex hematological disease characterized by genetic and clinical heterogeneity. The identification and understanding of chromosomal abnormalities are important for the diagnosis and management of AML patients. Compared with recurrent chromosomal trans...
Gespeichert in:
| Veröffentlicht in: | Mol Cytogenet |
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| Hauptverfasser: | , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7448493/ https://ncbi.nlm.nih.gov/pubmed/32863883 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-020-00507-0 |
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