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Acute myeloid leukaemia with t(8;21)(q22;q22.3) and loss of the X chromosome
Cytogenetic abnormalities occur in approximately 60% of newly diagnosed patients with acute myeloid leukaemia (AML) and are useful in the risk stratification of AML. Translocation between chromosomes 8 and 21—t(8;21)—(q22;q22.3), which carries a favourable prognosis, is found in approximately 5% to...
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| Vydáno v: | BMJ Case Rep |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4533636/ https://ncbi.nlm.nih.gov/pubmed/26250367 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2015-210855 |
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