4p16.3

A chromosome band present on 4p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1979-2017
05101519792017

Papers overview

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Highly Cited
2013
Highly Cited
2013
FGF receptor 3 (FGFR3) is activated by mutation or over-expression in many bladder cancers. Here, we identify an additional… (More)
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Highly Cited
2010
Highly Cited
2010
Previously, we reported germline DNA variants associated with risk of urinary bladder cancer (UBC) in Dutch and Icelandic… (More)
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Highly Cited
2010
Highly Cited
2010
We conducted a multi-stage, genome-wide association study of bladder cancer with a primary scan of 591,637 SNPs in 3,532 affected… (More)
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2001
2001
4p16.3 has previously been identified as a region of non-random LOH in transitional cell carcinoma, suggesting the presence of a… (More)
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1995
1995
Mapping genes for nonsyndromic hereditary hearing impairment may lead to identification of genes that are essential for the… (More)
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Highly Cited
1994
Highly Cited
1994
Achondroplasia (ACH) is the most common genetic form of dwarfism. This disorder is inherited as an autosomal dominant trait… (More)
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Highly Cited
1994
Highly Cited
1994
BACKGROUND Huntington's disease is associated with an expanded sequence of CAG repeats in a gene on chromosome 4p16.3. However… (More)
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Highly Cited
1994
Highly Cited
1994
Achondroplasia, the most common cause of chondrodysplasia in man (1 in 15,000 live births), is a condition of unknown origin… (More)
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Highly Cited
1993
Highly Cited
1993
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have used haplotype analysis of… (More)
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1992
1992
Within the Huntington's disease (HD) candidate region of 4p16.3, the D4S127 locus displays strong linkage disequilibrium with the… (More)
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