Unbalanced translocation t (5; 17) in an atypical acute promyelocytic leukemia

V Brunel, D Sainty, N Carbuccia… - Genes …, 1995 - Wiley Online Library
Acute promyelocytic leukemia (APL; M3 in the FAB classification) is specifically associated
with the t (15; 17)(q23; q12) and the consequent formation of a PML/RARA fusion gene. A …

A PML/RARA chimeric gene on chromosome 12 in a patient with acute promyelocytic leukemia (M4) associated with a new variant translocation: t(12;15;17)(q24;q24; …

A Bennour, I Tabka, YB Youssef, M Zaier, S Hizem… - Medical Oncology, 2013 - Springer
Acute promyelocytic leukemia (APL) is genetically characterized by a reciprocal
translocation between chromosomes 15 and 17, t (15; 17)(q22; q21), which results in the …

Masked t (15; 17) APL with the insertion of PML–RARα fusion gene in 4q21

K Haraguchi, N Ohno, M Tokunaga, M Tokunaga… - Leukemia research, 2009 - Elsevier
Most cases of acute promyelocytic leukemia (APL) are characterized by the reciprocal
translocation t (15; 17); however, several complex variant translocations have also been …

Variant complex translocations involving chromosomes 1, 9, 9, 15 and 17 in acute promyelocytic leukemia without RARα/PML gene fusion rearrangement

SK Gogineni, HO Shah, M Chester, JH Lin, M Garrison… - Leukemia, 1997 - nature.com
Acute promyelocytic leukemia (APL; M3) is specifically characterized by a predominance of
malignant promyelocytes having atypical reciprocal translocation involving chromosome 15 …

Molecular analysis of simple variant translocations in acute promyelocytic leukemia

J Borrow, K Howe, A Goddard… - Genes …, 1994 - Wiley Online Library
The primary cytogenetic abnormality in acute promyelocytic leukemia (APL; FAB M3) is a
reciprocal translocation, t (15; 17)(q22; q12), which serves to fuse the PML gene on …

A t (17; 20)(q21; q12) masking a variant t (15; 17)(q22; q21) in a patient with acute promyelocytic leukemia

Z García-Casado, J Cervera, A Valencia… - Cancer genetics and …, 2006 - Elsevier
Acute promyelocytic leukemia (APL) is genetically characterized by a reciprocal
translocation between chromosomes 15 and 17, the t (15; 17)(q22; q21), which results in the …

A new variant translocation of t (15; 17) in a patient with acute promyelocytic leukemia (M3): t (15; 19; 17)(q22; p13; q12)

K Saitoh, I Miura, Y Kobayashi, M Kume… - Cancer genetics and …, 1998 - Elsevier
The reciprocal translocation (15; 17) is specifically associated with acute promyelocytic
leukemia [APL; M3 subtype according to French-American-British (FAB) classification]. A few …

The genetic characterization of acute promyelocytic leukemia with cryptic t (15; 17) including a new recurrent additional cytogenetic abnormality i (17)(q10)

M Kim, J Lim, Y Kim, K Han, DH Lee, NG Chung, B Cho… - Leukemia, 2008 - nature.com
It is important to detect PML/RARa rearrangement in patient with morphologic acute
promyelocytic leukemia (APL). Rare cases of APL lacking the classic t (15; 17) on routine …

An eight-way variant t (15; 17) in acute promyelocytic leukemia elucidated using fluorescence in situ hybridization

LR Hiorns, GJ Swansbury, D Catovsky - Cancer genetics and cytogenetics, 1995 - Elsevier
A complex eight-way translocation was identified, with the aid of fluorescence in situ
hybridization (FISH), in a patient diagnosed as having acute promyelocytic leukemia (APL) …

A novel t (3; 17)(p25; q21) variant translocation of acute promyelocytic leukemia with rearrangement of the RARA locus

RL Redner, LC Contis, F Craig, C Evans, ME Sherer… - Leukemia, 2006 - nature.com
The vast majority of patients with acute promyelocytic leukemia (APL, FAB M3) have the t
(15; 17)(q22; q21) chromosomal translocation (reviewed in Melnick and Licht1). This …