Abstract The chromosome aberration t (7; 11)(p15; p15) is uncommon but recurrent in
leukemia. We experienced a case of acute leukemia with t (7; 11)(p15; p15), the …

Acute myeloid leukemia (AML) with NUP98-HOXA9 fusion gene is rare, which is caused by t
(7; 11)(p15; p15). Not only the prognosis is poor, the efficacy of conventional induction …

The t (7; 11)(p15; p15) translocation is a recurrent aberration observed in acute myeloblastic
leukaemia (AML) and chronic myelogenous leukaemia (CML). It has been shown that the …

We encountered a patient with Philadelphia‐negative chronic myeloid leukaemia, witht (7;
11)(p15; p15), in whom acute leukaemia phase (acute myeloid leukaemia‐M2 morphology) …

A 22-year-old woman presented with lymphadenopathy in a similar manner as she had
presented at age 4. At age 4, she was diagnosed with acute myelogenous leukemia (AML) …

Introduction Chromosomal rearrangements involving NUP 98 gene have been associated
with human leukemias such as de novo AML, therapy‐related AML (t‐AML), myelodysplastic …

Rare chronic myelogenous leukemia (CML) patients manifested as the primary blast phase
without a chronic and accelerated phase. The occurrence of at (8; 21) translocation in …

We report two additional patients with acute myeloid leukemia (AML) and a translocation
between chromosomes 7 and 11: t (7; 11)(p15; p15). One patient was diagnosed as having …

We report a 29-year-old Japanese male with acute myelogenous leukemia (AML)-M4 with a
cryptic t (7; 11)(p15; p15), in which a chimeric NUP98-HOXA9 fusion was detected by …

A 29-year-old woman having acute myelogeneous leukemia-M1 subtype with the
chromosomal abnormality t (16; 21)(p11; q22) is presented. Complete blood count at onset …