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t(12;21)

A cytogenetic abnormality that involves a translocation between chromosomes 12 and 21.
National Institutes of Health

Papers overview

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Highly Cited
2006
Highly Cited
2006
BackgroundTraditional methods of analysing gene expression data often include a statistical test to find differentially expressed… 
Highly Cited
2006
Highly Cited
2006
Purpose: To examine cancer genes undergoing epigenetic inactivation in a set of ETV6/RUNX1-positive acute lymphoblastic leukemias… 
Highly Cited
2003
Highly Cited
2003
Constitutive phosphorylation of Akt/PKB protein in acute myeloid leukemia: its significance as a prognostic variable 
Review
2001
Review
2001
Highly Cited
1999
Highly Cited
1999
Because previous PCR‐based methodologies for detection of minimal residual disease (MRD) in leukemia patients have been too… 
Highly Cited
1999
Highly Cited
1999
The t(12;21)(p13;q22) is a cryptic abnormality observed in 25% of children with B-lineage acute lymphoblastic leukemia (ALL… 
Highly Cited
1999
Highly Cited
1999
ABSTRACT t(12;21) is the most frequent translocation found in pediatric B-cell acute lymphoblastic leukemias. This translocation… 
Highly Cited
1997
Highly Cited
1997
The presence of ETV6 deletions was investigated in 215 children with acute lymphoblastic leukemia (ALL) using the loss of…