Unbalanced translocations, which are created if one of the two derivative chromosomes is
lost, often result in the loss or gain of chromosomal material rather than the formation of …

Cytogenetic abnormalities are observed in approximately two‐thirds of patients with acute
myeloid leukemia (AML). Chromosome rearrangements are associated with specific …

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 …

We report a case of acute myeloid leukemia (AML) M1 showing a 48, XY,+ 13,+ 13
karyotype. Treatment was according to the Medical Research Council AML14 trial protocol …

Abstract Acute Myelogeneous Leukemia (AML) is a heterogeneous disease with respect to
morphology, immunophenotype, and genetic rearrangements. Multiple recurrent …

No chromosomal rearrangements have been identified as specifically associated with
minimally differentiated acute myeloid leukemia (AML-M0). Several research groups studied …

Although the translocation (8; 21) is the single most common structural rearrangement
reported in acute myeloblastic leukemia (AML), it is rarely seen in AML FAB type M5. We …

Background/Aim: Acute myeloid leukemia is well characterized by chromosomal aberrations
that correspond to various subtypes of acute leukemias. The t (8; 21)(q22; q22) is a frequent …

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 …

We present a unique case of a young woman with acute myeloid leukemia (AML) with
complex karyotype. The presence of the t (4; 11)(q23; p15) is extremely rare in myeloid …