Jumping translocation (JT) is a cytogenetic event in which a donor chromosomal segment is
translocated to two or more recipient chromosomes. We describe a case of a 75-year-old …

The translocation t (8; 21) is one of the most common cytogenetic abnormalities in acute
myeloid leukemia (AML). It is closely associated with the French–American–British (FAB) …

The authors report two cases of secondary myelodysplasia and acute myeloid leukemia with
t (3; 21)(q26. 3; q22) as the only cytogenetic abnormality in neoplastic bone marrow. This …

Sex chromosomes are infrequently involved in patients with hematologic malignancies. In
most instances, the abnormality is either duplication in the q arm or deletion and …

We report a case of a patient aged about 53 years, who initially presented with
hematological disorders (WBC: 44000/mm3, Hb: 11g/dl, Pit: 127000/mm3) without tumoral …

Patients with normal-karyotype acute myelogenous leukemia (NKAML) may have
undetected genetic abnormalities that could affect prognosis. Screening for known AML …

A case of acute lymphoblastic leukemia with a new translocation, t (5; 9)(q22; q34) is
reported with special reference to the clinical features and the response to treatment. This …

Forty-three patients with acute myelogenous leukemia (AML) and a translocation 8; 21 were
reviewed. The patients' median age was 30 years, and 62% were men. Twenty-three …

One of the most frequent structural chromosomal anomaly is t (8; 21)(q22; q22) that occurs in
approximately 5-15% of all acute myeloid leukemia (AML). However, t (3; 21)(p21; q22) and …

We present a series of 12 cases of de novo acute lymphoblastic leukemia (ALL) with
translocation t (14; 18)(q32; q21). The median age of patients at presentation was 65.5 …