The boy, was detected with acute promyelocytic leukaemia (APL) and studies revealed PML-
retinoic acid receptor-α (RARA) rearrangement in 70% of 200 interphase nuclei, post initial …

Objective To investigate the clinical and laboratory characteristics of acute myeloid leukemia
(AML) with t (16; 21)(p11; q22) translocation. Methods Two patients diagnosed by …

Acute myeloid leukemia is classified based upon recurrent cytogenetic abnormalities. The t
(15; 17)(q24. 1; q21. 1) abnormality is found in 5% to 8% of de novo acute myeloid leukemia …

SHORT COMMUNICATION t(9;11)(p22;q24) in a Patient with Acute Monocytic Leukemia Page 1
SHORT COMMUNICATION t(9;11)(p22;q24) in a Patient with Acute Monocytic Leukemia N …

The translocation (8; 21)(q22; q22) is a frequent karyotypic abnormality in acute
myelogenous leukemia (AML). Most cases of AML with t (8; 21) show an M2 phenotype …

Balanced translocation between chromosomes 3q26 and 8q24 is a very rare event. Here we
report six patients with t (3; 8)(q26; q24) either as a sole or as a part of genetic abnormalities …

Chromosome 21 and in particular band 21q22, the site of AML1 (RUNX1, CBFA2) gene, is
among the most frequent targets of chromosomal translocations in leukemia observed in …

Abstract The translocation (6; 9)(p23; q34) is a rare cytogenetic aberration found in patients
with acute myeloid leukemia (AMD. The clinical, morphologic, and immunophenotypic …

Acute myelogenous leukemia (AML) with the translocation t (6; 9)(p23; q34) is a rare
disease entity with a poor prognosis. We report three patients; two were diagnosed with AML …

This case presents a Caucasian girl diagnosed with early pre-B cell acute lymphoblastic
leukemia at age 2 years. The only chromosomal anomaly detected in her bone marrow cells …