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 …

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 chromosome aberration t (7; 11)(p15; p15) is uncommon but recurrent in
leukemia. We experienced a case of acute leukemia with t (7; 11)(p15; p15), the …

The present study reviewed three patients with acute myeloid leukemia (AML) who had the
specific genetic abnormality t (16; 21)(p11; q22). To investigate the clinical and laboratory …

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 …

A 16-year-old Japanese woman with acute myelogenous leukemia (AML) and t (6; 9)
received peripheral blood stem cell transplantation (PBSCT). Although chromosomal studies …

Over a period of 14 years, 50 patients (12 children and 38 adults) of whom 46 had acute
myeloid leukemia (AML) and 4 had myelodysplastic syndrome characterized by the t (8; …

Acute leukemia with t (4; 12)(q11–13; p12–13) is rare but has unique characteristics. The
incidence of t (4; 12) in acute leukemias was about 0.6% in our laboratory. Twelve patients …

Acute myeloid leukemia with t (8; 21)(q22; q22) is a distinct type of leukemia considered to
have a favorable prognosis. However, some patients rapidly succumb to disease despite …

A 20-year-old female with Ph+ acute myelogenous leukemia (M2) associated with t (7;
11)(p15; p15) is reported. Bone marrow aspirates were hypercellular with leukemic cells …