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4p16.3

A chromosome band present on 4p
National Institutes of Health

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… Expand
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Review
2011
Review
2011
Huntington's disease is a progressive, fatal, neurodegenerative disorder caused by an expanded CAG repeat in the huntingtin gene… Expand
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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… Expand
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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… Expand
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Highly Cited
2004
Highly Cited
2004
Wolf-Hirschhorn syndrome is a multiple malformation syndrome with distinct abnormal craniofacial features, prenatal onset growth… Expand
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Highly Cited
2001
Highly Cited
2001
4p16.3 has previously been identified as a region of non-random LOH in transitional cell carcinoma, suggesting the presence of a… Expand
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Highly Cited
1999
Highly Cited
1999
Cherubism is a rare familial disease of childhood characterized by proliferative lesions within the mandible and maxilla that… Expand
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Highly Cited
1998
Highly Cited
1998
Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of… Expand
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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… Expand
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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… Expand
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