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19q13.2

A chromosome band present on 19q
National Institutes of Health

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Highly Cited
2012
Highly Cited
2012
Oligodendroglioma is characterized by unique clinical, pathological, and genetic features. Recurrent losses of chromosomes 1p and… Expand
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Highly Cited
2009
Highly Cited
2009
We report a prostate cancer genome-wide association follow-on study. We discovered four variants associated with susceptibility… Expand
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Highly Cited
2008
Highly Cited
2008
Kawasaki disease is a pediatric systemic vasculitis of unknown etiology for which a genetic influence is suspected. We identified… Expand
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Highly Cited
2004
Highly Cited
2004
Lung cancer is the most common fatal cancer among Danish men, and the incidence rate is increasing among women. In a case-cohort… Expand
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Highly Cited
2003
Highly Cited
2003
The new genetic information, in particular the greatly increased density of markers in the chromosomal maps, may permit analysis… Expand
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Highly Cited
2003
Highly Cited
2003
Alterations of 19q13 are frequently observed in glial neoplasms, suggesting that this region harbors at least one gene involved… Expand
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Highly Cited
2003
Highly Cited
2003
A number of chromosomal abnormalities including 19q deletions have been associated with the formation of human gliomas. In this… Expand
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Review
2000
Review
2000
Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene which encodes a protein… Expand
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Highly Cited
1994
Highly Cited
1994
An association between the 19q13.2 chromosomal region and Alzheimer's disease (AD) has been reported in AD families and for… Expand
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Highly Cited
1993
Highly Cited
1993
Apolipoprotein E is immunochemically localized to the senile plaques, vascular amyloid, and neurofibrillary tangles of Alzheimer… Expand
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