17q11

A chromosome band present on 17q
National Institutes of Health

Papers overview

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2011
2011
MicroRNAs (miRNAs) are small non-coding RNA molecules that are often located in genomic breakpoint regions and can act as… (More)
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Review
2009
Review
2009
Autism spectrum disorders (ASDs) are a clinically complex group of childhood disorders that have firm evidence of an underlying… (More)
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Highly Cited
2008
Highly Cited
2008
Chromosomal rearrangements that create gene fusions are common features of human tumors. The prevailing view is that the… (More)
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Highly Cited
2008
Highly Cited
2008
Propensity for subsequent distant metastasis in head and neck squamous-cell carcinoma (HNSCC) was analysed using 186 primary… (More)
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Highly Cited
2005
Highly Cited
2005
Autism is a heritable but genetically complex disorder characterized by deficits in language and in reciprocal social… (More)
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Highly Cited
2004
Highly Cited
2004
We investigated the genetic aspects of the large sex bias in the prevalence of autism spectrum disorder by monitoring changes in… (More)
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2004
2004
Chromosome 22q11.2 deletions are found in almost 90% of patients with DiGeorge/velocardiofacial syndrome (DGS/VCFS). Large… (More)
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2002
2002
  • S Luoh
  • Cancer genetics and cytogenetics
  • 2002
Amplification of a portion of 17q11 approximately q12 involving the human epidermal growth factor receptor-2 (HER-2/neu) gene is… (More)
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1998
1998
Bladder cancer progression is thought to be associated with sequential genetic events. To search for the specific genetic changes… (More)
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1992
1992
Type I neurofibromatosis (NF1) is a common autosomal dominant disorder that affects tissues derived from the neural crest. The… (More)
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