The reciprocal translocation between chromosomes 8 and 21 with breakpoints in 8q22 and
21q22 was first reported by Rowley, in 1973, 1 in a subgroup of patients with acute myeloid …

A 43-year-old male developed acute myelogenous leukemia (AML, M5b) with an acquired
Robertsonian 13; 15 translocation. He did not achieve complete remission after sequential …

The t (8; 21) abnormality occurs in a minority of acute myeloid leukemia (AML) patients. The
translocation results in an in‐frame fusion of two genes, resulting in a fusion protein of one N …

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 …

We describe a 65-year old woman who developed at (8; 16)(p11; p13) positive acute
myeloid leukemia (AML)-M4 without a prior myelodysplasia thirty-six months after a low …

Following reports of childhood acute myeloid leukemia (AML) showing that patients with t (9;
11)(p22; q23) have a better prognosis than those with translocations between 11q23 and …

We report two cases of secondary acute lymphoblastic leukemia (ALL) with t (4; 11)(q21;
q23) translocation occurring after chemotherapy and radiotherapy for a prior cancer. Seven …

The classification of acute myeloid leukemia (AML) recognizes a subgroup of diseases with
recurring genetic abnormalities. Translocation (15; 17) is the marker of acute promyelocitic …

Purpose Acute myeloid leukemia (AML) with translocation (t)(8; 21) or inversion (inv)(16) is
associated with a favorable prognosis when treated with intensive chemotherapy. In elderly …

The complex variants of t (8; 21) involving chromosomes 8 and 21 as well as a variable
chromosome account for 1.1∼ 5% of acute myeloid leukemia (AML) patients. This paper …