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21q22.2

A chromosome band present on 21q
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
Different types of genetic technologies and approaches allow for the study and identification of different types of genetic… Expand
Highly Cited
2009
Highly Cited
2009
Androgen signaling facilitates the formation of an oncogenic fusion gene in prostate cancer cells. Gene fusions play a critical… Expand
Highly Cited
2006
Highly Cited
2006
Prostate cancer is a common and clinically heterogeneous disease with marked variability in progression. The recent… Expand
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Highly Cited
2006
Highly Cited
2006
Among the various phenotypes seen in Down syndrome (DS), mental retardation is the most common and most debilitating condition… Expand
Highly Cited
1998
Highly Cited
1998
Down syndrome (DS), a major cause of mental retardation, is characterized by subtle abnormalities of cortical neuroanatomy… Expand
Highly Cited
1997
Highly Cited
1997
Using Down syndrome as a model for complex trait analysis, we sought to identify loci from chromosome 21q22.2 which, when present… Expand
Highly Cited
1996
Highly Cited
1996
The presence of an extra copy of human chromosome 21 (trisomy 21), especially region 21q22.2, causes many phenotypes in Down… Expand
1996
1996
We identified and cloned a novel 9,078-bp cDNA, designated TPRDI, from the Down syndrome-critical region by exon trapping. The… Expand
Highly Cited
1995
Highly Cited
1995
  • D J Smith, Y Zhu, J Zhang, J F Cheng, E. Rubin
  • Genomics
  • 1995
  • Corpus ID: 3052508
Libraries of the entire human genome, or regions of the genome, have been made in bacteria, yeast, and somatic cells. We have… Expand
Highly Cited
1989
Highly Cited
1989
The duplication of a specific region of chromosome 21 could be responsible for the main features of Down syndrome. To define and… Expand