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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...

詳細記述

保存先:
書誌詳細
出版年:BMJ Case Rep
主要な著者: Mohamed, Muhajir, Dun, Karen
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Publishing Group 2015
主題:
オンライン・アクセス: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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