Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

16q22.2

A chromosome band present on 16q
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
BackgroundGene innovation by duplication is a fundamental evolutionary process but is difficult to study in humans due to the… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • table 1
Is this relevant?
Highly Cited
2012
Highly Cited
2012
Malaria causes approximately one million fatalities per year, mostly among African children. Although highlighted by the strong… Expand
  • figure 1
  • table 1
  • figure 2
Is this relevant?
2010
2010
BACKGROUND & AIMS Ten common low-penetrant genetic variants have been consistently associated with colorectal cancer (CRC) risk… Expand
Is this relevant?
Highly Cited
2008
Highly Cited
2008
Chromosome region 1q21.1 contains extensive and complex low-copy repeats, and copy number variants (CNVs) in this region have… Expand
  • table 2
  • figure 1
  • figure 2
  • figure 4
Is this relevant?
Highly Cited
2008
Highly Cited
2008
Breast carcinomas are characterized by DNA copy number alterations (CNAs) with biological and clinical significance. This… Expand
  • figure 1
  • figure 2
  • figure 3
  • table 1
  • figure 4
Is this relevant?
2006
2006
The HYDIN gene located in human chromosome band 16q22.2 is a large gene encompassing 423 kb of genomic DNA that has been… Expand
Is this relevant?
2003
2003
Posterior polar cataracts are relatively uncommon yet they pose a significant challenge to the cataract surgeon. Cataract surgery… Expand
Is this relevant?
2002
2002
Ovarian cancer (OC) is often asymptomatic at the initial stage. When diagnosed, up to 75% of the patients present grade III or IV… Expand
Is this relevant?
2001
2001
Cancer cell lines are essential gene discovery tools and have often served as models in genetic and functional studies of… Expand
Is this relevant?
1998
1998
Cancer is a genetic disease resulting from an accumulation of genetic abnormalities in various regulatory genes. Most studies on… Expand
  • table I
  • table 2
  • figure 2
Is this relevant?