The t(1;19)(q23;p13.3) is one of the most common chromosomal abnormalities in B-cell precursor acute lymphoblastic leukemia (BCP-ALL) and usually gives rise to the TCF3/PBX1 fusion gene.
Tumors
ALL (5%)
LMNH ANLL
Molecular biology
PBX1E/E2A fusion gene
See also
Oncobase
ALL (5%)