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Dear Editor, Isochromosome 17 [i(17)(q10)] is a karyotypic abnormality observed in myeloid disorders mainly during disease evolution to acute myeloid leukaemia (AML) in Philadelphiapositive chronic myeloid leukaemia (CML). It has been reported in rare cases of myelodysplastic syndrome (MDS), with an incidence of 0.4–1.57 % [1, 2]. It is considered as a rare(More)
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