The translocation t (8; 16)(p11; p13), which results in fusion of the MOZ/MYST3/KAT6A gene
(8p11) and CBP/CREBBP gene (16p13), is characterized by unique morphologic and …

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 …

Abstract The t (8; 16)(p11; p13) fuses the MOZ (MYST3) gene at 8p11 with CBP (CREBBP)
at 16p13 and is associated with an infrequent but well‐defined type of acute myeloid …

The reciprocal chromosomal rearrangement t (8; 16)(p11; p13) is rare both in adult and
pediatric acute myeloid leukemias (AML) accounting 0.2–0.4% of de novo AML and 6.5% of …

Abstract The translocation t (8; 16)(p11; p13) is associated with a subtype of acute monocytic
leukemia (AML M5) characterized morphologically by erythrophagocytosis and clinically by …

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 …

Adult acute myeloid leukemia (AML) with t (8; 16)(p11; p13) is a rare subgroup with a poor
prognosis. However, Coenen et al.[1] reported that spontaneous remission occurred in 7 of …

Chromosome translocations that result in gene fusion and expression of the fusion gene
products are frequently observed in acute myeloid leukemia (AML). The recurrent …

Abstract The t (8; 16)(p11; p13), which is strongly associated with acute myeloid leukemia
(AML) displaying monocytic differentiation, erythrophagocytosis by the leukemic cells, and a …

Acute myeloid leukemia (AML) with t (8; 16)(p11; p13) is known to have very poor prognosis
in adults. In contrast, the prognosis is not clear in pediatric patients and chemotherapy is …