13q14.3

A chromosome band present on 13q
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Non-coding RNAs are much more common than previously thought. However, for the vast majority of non-coding RNAs, the cellular… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2008
2008
BACKGROUND AND OBJECTIVE Monoallelic deletion of 13q14.3 (13q14x1) is the most common abnormality in chronic lymphocytic leukemia… (More)
  • table 1
  • figure 1
  • table 2
  • table 3
  • table 4
Is this relevant?
Highly Cited
2006
Highly Cited
2006
Genome-wide microarray-based comparative genomic hybridization (array CGH) was used to identify common chromosomal alterations… (More)
  • table 1
  • table 2
  • figure 1
  • table 3
  • table 4
Is this relevant?
Review
2003
Review
2003
Wilson disease is an inherited autosomal recessive disorder of hepatic copper metabolism leading to copper accumulation in… (More)
Is this relevant?
2002
2002
Loss of genomic material from chromosomal band 13q14.3 is the most common genetic imbalance in B-cell chronic lymphocytic… (More)
  • figure 2
  • figure 3
  • figure 4
  • figure 5
  • figure 6
Is this relevant?
2001
2001
Deletion of the 13q14 chromosomal region is frequent in B cell chronic lymphocytic leukemia (B-CLL) and is believed to inactivate… (More)
  • figure 1
  • figure 2
  • figure 3
  • table 1
  • figure 4
Is this relevant?
1999
1999
We studied loss of heterozygosity (LOH) on human chromosome 13q in prostate cancer specimens to determine the location of a… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • table 1
Is this relevant?
1998
1998
A region of chromosome 13q14.3, telomeric to the Retinoblastoma gene RB-1 is frequently deleted in patients with B-cell chronic… (More)
  • figure 1
  • figure 2
  • figure 4
  • table 1
  • figure 5
Is this relevant?
Highly Cited
1993
Highly Cited
1993
Wilson disease (WD) is an autosomal recessive disorder characterized by the toxic accumulation of copper in a number of organs… (More)
Is this relevant?
Highly Cited
1993
Highly Cited
1993
Wilson disease (WD) is an autosomal recessive disorder of copper transport which maps to chromosome 13q14.3. In pursuit of the WD… (More)
Is this relevant?