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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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BMJ Case Rep
Egile Nagusiak: Mohamed, Muhajir, Dun, Karen
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BMJ Publishing Group 2015
Gaiak:
Sarrera elektronikoa: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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