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Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype
BACKGROUND: Acute myeloid leukemia is a clonal hematopoietic malignant disease; about 45–50% of cases do not have detectable chromosomal abnormalities. Here, we identified hidden genomic alterations and novel disease-related regions in normal karyotype acute myeloid leukemia/myelodysplastic syndrome...
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| Main Authors: | , , , , , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Ferrata Storti Foundation
2009
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2635399/ https://ncbi.nlm.nih.gov/pubmed/19144660 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.13024 |
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