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17q21.3

A chromosome band present on 17q
National Institutes of Health

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Highly Cited
2014
Highly Cited
2014
Copy number variants (CNVs) are risk factors in neurodevelopmental disorders, including autism, epilepsy, intellectual disability… Expand
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Highly Cited
2011
Highly Cited
2011
BackgroundTo date, nine Parkinson disease (PD) genome-wide association studies in North American, European and Asian populations… Expand
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Highly Cited
2006
Highly Cited
2006
Recently, the application of array-based comparative genomic hybridization (array CGH) has improved rates of detection of… Expand
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Highly Cited
2002
Highly Cited
2002
Genetic changes underlie tumor progression and may lead to cancer-specific expression of critical genes. Over 1100 publications… Expand
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Highly Cited
2000
Highly Cited
2000
Human UDP-d-xylose:proteoglycan core protein beta-d-xylosyltransferase (EC 2.4.2.26, XT-I) initiates the biosynthesis of… Expand
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Highly Cited
1998
Highly Cited
1998
BACKGROUND Multidrug resistance-associated protein (MRP) and canalicular multispecific organic anion transporter (cMOAT) are… Expand
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Highly Cited
1997
Highly Cited
1997
The unstable proteins Cdc6p and cdc18+ are essential and rate limiting for the initiation of DNA replication in Saccharomyces… Expand
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Highly Cited
1996
Highly Cited
1996
The chromosome localization of human HOX gene clusters has been reinvestigated by fluorescence in situ hybridization (FISH… Expand
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1993
1993
Using 11 restriction fragment length polymorphism markers, we examined loss of heterozygosity on the long arm of chromosome 17… Expand
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1993
1993
From chromosomal region 17q21.3, where a tumour suppressor gene(s) for breast and ovarian cancers is thought to be present, we… Expand
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