AML1-MTG16 fusion gene in therapy-related acute leukemia with t (16; 21)(q24; q22); two new cases

F Salomon-Nguyen, BL Coniat, M Lafage Pochitaloff… - Leukemia, 2000 - nature.com
Among the abnormalities of chromosomal band 21q22 associated with therapy-induced
leukemia, the rare but recurrent t (16; 21)(q24; q22) translocation has been reported to …

[HTML][HTML] Acute myeloid leukemia harboring t (8; 21)(q22; q22): a heterogeneous disease with poor outcome in a subset of patients unrelated to secondary cytogenetic …

P Lin, L Chen, R Luthra, SN Konoplev, X Wang… - Modern pathology, 2008 - Elsevier
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 …

[HTML][HTML] A Novel Cytogenetic Variant Translocation in Acute Myeloid Leukemia

MV Patel, SN Vaniawala, PK Gadhia - Journal of Case Reports, 2017 - casereports.in
Background: Acute myeloid leukemia (AML) is a heterogeneous group of malignant
neoplasm of hematopoietic disorders characterized by an abnormal proliferation of myeloid …

[引用][C] A novel translocation, t (3; 20)(q13; p13), in acute monocytic leukemia

B Qian, Z Sun, Z Wu, H Liu… - Cancer genetics and …, 2009 - cancergeneticsjournal.org
Because an increasing number of chromosomal aberrations have been detected in the
patients with acute leukemia, cytogenetic findings have become more valuable in …

Translocation (12; 17)(q13; q23) in de novo acute myeloid leukemia with trilineage myelodysplasia

KF Wong, CC So, PH Yu - Cancer genetics and cytogenetics, 1999 - Elsevier
12q13 abnormalities have been reported to be associated with a variety of benign and
malignant solid tumors. Recently, they have been shown to be a nonrandom karyotypic …

De novo acute myelogenous leukemia with trilineage myelodysplasia associated with t (8; 21)(q22; q22)

S Fujisawa, J Togawa, M Tanaka… - Internal …, 1999 - jstage.jst.go.jp
Wedescribe a rare case of de novoacute myelogenousleukemia with trilineage
myelodysplasia (AML/TMDS) associated with t (8; 21)(q22; q22). The patient was admitted to …

Acute leukemia with t (10; 11)(p11-p15; q13-q23)

C Secco, PH Wiernik, JM Bennett, E Paietta - Cancer genetics and …, 1996 - Elsevier
We report six patients with acute leukemia characterized by the presence of at (10; 11)(p11-
p15; q13-q23), either as sole cytogenetic abnormality (three patients) or as part of a complex …

MLL partial tandem duplications in acute leukemia cell lines

H Quentmeier, J Reinhardt, M Zaborski, HG Drexler - Leukemia, 2003 - nature.com
Recurrent translocations involving the MLL gene on chromosome band 11q23 together with
diverse partners have been reported in both acute myeloid leukemia (AML) and acute …

[引用][C] A novel t (7; 13)(p12; q33∼ q34) in AML-M2

E Gerbino, C Tapinassi, O Malazzi… - Cancer genetics …, 2009 - cancergeneticsjournal.org
Chromosomal rearrangements in acute myeloid leukemia (AML) frequently give rise to
aberrant transcripts, generating corresponding fusion proteins that are responsible for …

A novel translocation (6;20)(q13;q12) in acute myeloid leukemia likely results in LMBRD1–CHD6 fusion

N Douet-Guilbert, E De Braekeleer, C Tous… - Leukemia & …, 2015 - Taylor & Francis
Deletion of the long arm of chromosome 20 is a recurrent abnormality identified in
myelodysplastic syndromes (MDS) and chronic myeloproliferative disorders (MPD)(http …