Translocations involving the EVI1/MDS1 gene at 3q26 and the TEL gene at 12p13 are
comparatively common in acute leukemia, but a translocation between the two genes has …

Chromosomal translocation often results in aberrant activation of the genes with oncogenic
potential and, thus, plays an important role in leukemogenesis. We report a unique case of …

The t (2; 8; 21) is a complex translocation of t (8; 21), and is very rare. To investigate the
laboratory characteristics of a complex translocation t (2; 8; 21)(p12; q22; q22) in a patient …

Abstract The t (3; 12)(q26; p13) translocation is a recurrent chromosomal aberration
observed in myeloid malignancies. It has been shown that the translocation results in the …

The purpose of this study is to examine the relationship of t (11; 16)(q23; p13) to the type of
myeloproliferative disorder noted by hematopathology. Previously, t (11; 16) has been …

Abstract A translocation (6; 11)(q26–27; q23) was detected in four male patients diagnosed
with acute T-cell lymphoblastic leukemia and acute myelomonocytic and monocytic …

Chromosome band 12p13 is known as a recurring site for cytogenetic alteration in a variety
of hematological malignancies such as acute lymphocytic leukemia (ALL), acute …

Objective To investigate the clinical and laboratory characteristics of a complex translocation
t (6; 21; 8)(p22; q22; q22) in two patients with acute myeloid leukemia. Methods Bone …

DEK-NUP214 is a recurrent, but relatively rare translocation in myeloid neoplasia ($0.7–2%)
1, 2 associated with a poor prognosis in acute myeloid leukemia (AML) and myelodysplastic …

We have identified a new recurrent reciprocal translocation between chromosome 3 and 12
with breakpoints at bands 3q26 and 12p13, t (3; 12)(q26; p13) in the malignant cells from …