Abstract The t (8; 16)(p11; p13) translocation, associated with poor prognosis acute
monocytic leukemia, fuses MYST3 on chromosome region 8p11 to CBP on chromosome …

We report a novel fusion of the MYST4 and CBP genes in an acute myeloid leukaemia
(AML)‐M4 patient exhibiting t (10; 16)(q22; p13) and t (11; 17)(q23; q21). The t (10; 16)(q22; …

Thirty cases of acute myeloid leukaemia (AML) with MYST histone acetyltransferase 3
(MYST3) rearrangement were collected in a retrospective study from 14 centres in France …

Abstract The translocation t (8; 16)(p11; p13) is associated with acute myeloid leukemia
displaying monocytic differentiation (AML FAB M4/5) and fuses the MOZ (also named …

Acute myeloid leukemia (AML) with translocation t (8; 16)(p11; p13) is an infrequent
leukemia subtype with characteristic clinicobiological features. This translocation leads to …

Abstract The t (8; 16)(p11; p13) is a rare translocation involved in de novo and therapy-
related myelomonocytic and monocytic acute leukemia. It fuses two genes encoding histone …

The t (10; 17)(p15; q21) translocation is a very rare but recurrent cytogenetic aberration in
acute myeloid leukemia (AML), which would be classified as AML, not otherwise specified …

A Chinese girl presented with generalized papular rash and monocytic leukemia 19 days
after birth. Cytogenetic analysis showed t (8; 16)(p11. 2; p13. 3) as the sole chromosomal …

Translocation (10; 17)(p15; q21) is a recurrent abnormality that has been reported in only
seven cases of acute leukemia, including two by our group [1](available at: http://cgap. nci …

Translocation t (8; 16)(p11; p13) involving the MOZ/MYST3 gene (8p11) and the
CBP/CREBBP gene (16p13) is associated with the FAB M4/M5 subtype of acute myeloid …