17q11.1

A chromosome band present on 17q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1993-2018
01219932018

Papers overview

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2010
2010
PURPOSE Several prognostic gene expression profiles have been identified in breast cancer. In spite of this progress in… (More)
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2010
2010
OBJECTIVE Prenatal diagnosis of small supernumerary marker chromosomes (sSMC) gives rise to difficulties in genetic counseling… (More)
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2006
2006
Gain of chromosome 17 is the most prevalent genetic abnormality identified in neuroblastoma (NB) and distal 17q gain has… (More)
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2003
2003
Congenital cataracts are an important cause of blindness worldwide. In a family of Chinese descent, a dominant congenital nuclear… (More)
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2003
2003
OBJECTIVE To identify the genetic defect causing automosal dominant congenital cataracts (ADCC) with nuclear opacities in a… (More)
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2000
2000
PURPOSE To map the locus for autosomal dominant cataracts (ADCs) in a Brazilian family using candidate gene linkage analyses… (More)
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1999
1999
By in situ chromosomal hybridization, and by somatic cell and radiation hybrid analysis, we have determined the genomic position… (More)
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1998
1998
BACKGROUND The serotonin transporter (5-HTT) is an important candidate gene for the genetic transmission of manic depressive… (More)
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1997
1997
Bleomycin hydrolase (BH) is the only known eukaryotic enzyme that inactivates the widely used antineoplastic agent bleomycin (BLM… (More)
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Highly Cited
1993
Highly Cited
1993
A Na(+)- and Cl(-)-coupled serotonin (5-hydroxytryptamine, 5HT) transporter is expressed on human neuronal, platelet, placental… (More)
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