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17q11

A chromosome band present on 17q
National Institutes of Health

Papers overview

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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… Expand
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Highly Cited
2007
Highly Cited
2007
We analyzed the subchromosomal numerical aberrations of 44 surgically resected pancreatic adenocarcinomas by array‐based… Expand
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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… Expand
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Highly Cited
2004
Highly Cited
2004
A large body of research supports a multifactorial cause in multiple sclerosis (MS), with an underlying genetic susceptibility… Expand
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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… Expand
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Highly Cited
2001
Highly Cited
2001
A novel human gene, SARM, encodes the orthologue of a Drosophila protein (CG7915) and contains a unique combination of the… Expand
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Highly Cited
1999
Highly Cited
1999
To search for recurrent and specific genomic alterations in human hepatocellular carcinoma (HCC), we examined 18 cell lines by… Expand
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Review
1999
Review
1999
  • M. Rothenberg
  • American journal of respiratory cell and…
  • 1999
  • Corpus ID: 18245564
Eosinophil accumulation in the peripheral blood and tissues is a hallmark feature of several important medical diseases… Expand
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Highly Cited
1997
Highly Cited
1997
The group of autosomal recessive (AR) muscular dystrophies includes, among others, two main clinical entities, the limb-girdle… Expand
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Highly Cited
1995
Highly Cited
1995
Congenital cataracts constitute a morphologically and genetically heterogeneous group of diseases that are a major cause of… Expand
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