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t(6;11)

A cytogenetic abnormality that involves a translocation between chromosomes 6 and 11.
National Institutes of Health

Papers overview

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Review
2013
Review
2013
Recently, a new category of MiTF/TFE family translocation carcinomas of the kidney has been proposed. This category includes Xp11… 
Review
1998
Review
1998
BACKGROUND AND OBJECTIVE The ALL1 gene, also referred to as MLL, HRX or Htrx1, is interrupted in the vast majority of… 
Highly Cited
1998
Highly Cited
1998
Seventeen cytogenetic laboratories in eight European countries contributed karyotypic, hematological, clinical and follow-up data… 
1997
1997
In infantile leukemias and therapy-related leukemias, the MLL gene is frequently found to be disrupted and fused to various… 
1996
1996
The t(6;11)(q27;q23) is one of the most common translocations observed in patients with acute myeloid leukemia (AML). The… 
Highly Cited
1992
Highly Cited
1992
Translocations involving 11q23 are recurring abnormalities in human acute leukemia cells of either lymphoid or myeloid lineage… 
1992
1992
The yeast artificial chromosome (YAC-13HH4), which spans a 440-kb region of DNA just distal to the CD3 locus on chromosome 11 at… 
1992
1992
The 11q23 chromosome band is frequently associated with chromosomal aberrations in human leukemias. We have previously cloned a… 
1991
1991
A new strategy for mapping chromosome translocation breakpoints in relation to known genes has been developed. This approach is… 
1990
1990
In situ hybridization was performed in a case of acute monoblastic leukemia (FAB type M5b) with a rearrangement of the long arm…