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t(1;19)

A cytogenetic abnormality that involves a translocation between chromosomes 1 and 19.
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
To evaluate the impact of contemporary therapy on the clinical outcome of children with pre-B acute lymphoblastic leukemia (ALL… 
Highly Cited
2006
Highly Cited
2006
Combined deletion of chromosomes 1p and 19q is associated with improved prognosis and responsiveness to therapy in patients with… 
Review
1999
Review
1999
Prospective studies on the detection of minimal residual disease (MRD) in acute leukemia patients have shown that large-scale MRD… 
Highly Cited
1991
Highly Cited
1991
The t(1;19) translocation that characterizes 25% of pediatric pre-B cell acute lymphoblastic leukemias (pre-B ALL) produces a… 
Highly Cited
1990
Highly Cited
1990
The prognostic significance of chromosomal translocations, particularly t(1;19) (q23;p13), was evaluated in children with pre-B… 
Highly Cited
1989
Highly Cited
1989
The gene (E2A) that codes for proteins with the properties of immunoglobulin enhancer binding factors E12/E47 was mapped to…