A case of acute myelogenous leukemia with an 8–21 translocation, missing Y, and additional karyotypic abnormalities

Y Kaneko, M Sakurai, M Hattori - American Journal of …, 1978 - Wiley Online Library
A patient with acute myelogenous leukemia (AML) whose bone marrow cells had
complicated chromosomal abnormalities, in addition to an 8–21 translocation and a missing …

Acute Myeloid Leukemia With t(6;9) (p23;q34): Association With Myelodysplasia, Basophilia, and Initial CD34 Negative Immunophenotype

R Alsabeh, RK Brynes, ML Slovak… - American journal of …, 1997 - academic.oup.com
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 …

Translocation t (6; 9)(p23; q34) in acute myeloid leukemia without myelodysplasia or basophilia: two cases and a review of the literature.

DM Lillington, PK MacCallum, TA Lister, B Gibbons - Leukemia, 1993 - europepmc.org
The clinical, hematological, and cytogenetic data from two young adults with acute myeloid
leukemia (AML) FAB type M1 is described. At diagnosis, cytogenetic investigation revealed …

Variant translocation t (8; 21; 15) in an acute myeloblastic leukemia with phenotypic differential evolution

N Ayraud, S Raynaud, J Bayle, P Dujardin - Cancer genetics and …, 1985 - Elsevier
A new case of a variant form of the translocation (8; 21) in an AML-M2, including in addition
involvement of chromosome# 15 is reported. The selection of two abnormal lines, probably …

Cytologic characterization and significance of normal karyotypes in t (8; 21) acute myeloblastic leukemia

R Berger, A Bernheim, MT Daniel, F Valensi, F Sigaux… - 1982 - ashpublications.org
A cytologic and cytogenetic study of 10 cases of acute myeloblastic leukemia with
maturation and t (8; 21) translocation is reported. Despite a certain polymorphic appearance …

[HTML][HTML] Characteristics of translocation (16; 16)(p13; q22) acute myeloid leukemia

A Eghtedar, G Borthakur, F Ravandi… - American journal of …, 2012 - ncbi.nlm.nih.gov
A subgroup of patients with core binding factor acute myeloid leuke-mias (AML) is
characterized by the presence of the fusion gene CBFb-Myh11. At the cytogenetic level …

Translocation t (9; 11)(p21; q23) in pediatric de novo and secondary acute myeloblastic leukemia.

C Sandoval, DR Head, J Mirro Jr, FG Behm, GD Ayers… - Leukemia, 1992 - europepmc.org
The t (9; 11)(p21; q23) has been associated with characteristic clinical features and a
superior treatment outcome in previously untreated pediatric acute myeloblastic leukemia …

[PDF][PDF] Structural rearrangements of chromosome 3 in 57 patients with acute myeloid leukemia: clinical, hematological and cytogenetic features

C Charrin, A Belhabri, D Treille-Ritouet… - The Hematology …, 2002 - researchgate.net
Results: Patients with myeloid malignancy displaying 3q rearrangement were assigned to
five subgroups, including those with: 3q21/q26 rearrangement; 3q21 alone, including t (1; …

Recurrent cytogenetic abnormalities in acute myeloid leukemia

JJ Yang, TS Park, TSK Wan - Cancer Cytogenetics: Methods and Protocols, 2017 - Springer
The spectrum of chromosomal abnormality associated with leukemogenesis of acute
myeloid leukemia (AML) is broad and heterogeneous when compared to chronic myeloid …

A translocation between 3q21 and 12q24 in a patient with minimally differentiated acute myeloid leukemia (AML-MO)

N Yamagata, C Shimazaki, T Kikuta, H Hirai… - Cancer genetics and …, 1997 - Elsevier
Only a small number of reports have described the cytogenetic analysis of minimally
differentiated acute myeloid leukemia (AML, MO). We performed a cytogenetic analysis on a …