We report two additional patients with acute myeloid leukemia (AML) and a translocation
between chromosomes 7 and 11: t (7; 11)(p15; p15). One patient was diagnosed as having …

Two patients with acute myelogenous leukemia (AML) are described. The first case is that of
a patient with AML who had a low leukocyte alkaline phosphatase level associated with a …

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 …

A case of acute myeloblastic leukemia (AML) of M2 type in the FAB classification without
Auer bodies in the leukemic cells was shown to have t (6; 9)(p23; q34) in the marrow cells …

The cellular and molecular genetic aberrations of hematopoietic and lymphoid tissues are
increasingly important in leukemia classification and are prognostically significant. Although …

Abstract t (8; 21)(q22; q22) is the most frequently observed karyotypic abnormality
associated with acute myeloid leukemia (AML), especially in FAB M2. Clinically, this type of …

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 …

We present an 18-year-old woman who was diagnosed with acute myeloblastic leukemia
(AML M2), and in whom chromosome analysis of bone marrow cells revealed t (7; 11), an …

The occurrence of trisomy 4 or trisomy 10 as the sole chromosomal abnormality in acute
myeloid leukemia (AML) is very rare, the reported frequency being less than 1%. We …

Nine acute myelogenous leukemia (AML) patients with a translocation 8; 21, who were
treated at Keio University Hospital between 1983 and August 1990, were reviewed. All of …