A 66-year-old Chinese man was admitted to our hospital in September 2006 because of
shortness of breath and palpitation after exertion, which was exacerbated and accompanied …

Discussion Translocation (16; 21)(p11; q22) is a uncommon but recurrent cytogenetic
abnormality described in acute myeloid leukaemia (AML) and one case of chronic myeloid …

Chromosomal rearrangements involving the MLL gene (approved symbol: KMT2A) at 11q23
are associated with different types of hematological malignancies, with more than 70 fusion …

DISCUSSION Specific cytogenetic abnormalities may involve balanced chromosomal
translocations, which lead to gene fusions and chimeric proteins with gene regulatory …

Cytogenetics has a pivotal role in risk stratification of acute myeloid leukemia (AML). We
report a case of AML with at (4; 12)(q12; p13). To the best of our knowledge, there are about …

A 29-year-old woman having acute myelogeneous leukemia-M1 subtype with the
chromosomal abnormality t (16; 21)(p11; q22) is presented. Complete blood count at onset …

The t (7; 11)(p15; p15) translocation is a recurrent genetic abnormality associated with acute
myelogenous leukemia (AML). The translocation results in a fusion between the nucleoporin …

Abstract The t (8; 21)(q22; q22) is the most common translocation in acute myeloid leukemia
(AML). We describe the clinicopathologic and cytogenetic profile of 117 patients with t (8; 21) …

Abstract The translocation (8; 21)(q22; q22) is commonly associated with acute myeloid
leukemia (AML) M2 according to the French‐American‐British (FAB) classification. We …