Cytogenetics is an indispensable tool for the diagnosis and prognosis of acute myeloid
leukaemia (AML). The t (8; 16)(p11; p13) chromosomes is rare in this pathology. This paper …

Résumé La cytogénétique constitue un outil indispensable pour le diagnostic et le pronostic
de la leucémie aigue myéloïde (LAM). La t (8; 16)(p11; p13) est rare au cours de cette …

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

Introduction Chromosomal translocations involving nucleoporin NUP98 protein have often
been described in acute myeloid leukemia (AML). Fusing NUP98 gene at chromosome 11 …

The classification of acute myeloid leukemia (AML) recognizes a subgroup of diseases with
recurring genetic abnormalities. Translocation (15; 17) is the marker of acute promyelocitic …

Recurrent genetic abnormalities are important prognostic markers in acute myeloid
leukemias (AML). The World Health Organization classification recognizes 7 categories of …

Aim: The translocation (6; 9)(p23; q34) is a rare cytogenetic aberration found in patients with
acute myeloid leukemia (AML)(about 1% of all AML), and correlates with poor clinical …

A case of acute monocytic leukemia (AMoL) with t (5; 11)(q31; q23) and a case of acute
myelomonocytic leukemia (AMMoL) with t (5; 11)(q35; q13. 1) are reported. The …

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 …

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 …