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19q13.31

A chromosome band present on 19q
National Institutes of Health

Papers overview

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2017
2017
Genome-wide association studies (GWAS) have discovered thousands loci associated with disease risk and quantitative traits, yet… Expand
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Highly Cited
2012
Highly Cited
2012
BackgroundSpecific genetic contributions for preeclampsia (PE) are currently unknown. This genome-wide association study (GWAS… Expand
Review
2011
Review
2011
Abstract The genetic origin of the three common variants of the human apolipoprotein E (apoE) protein, known as E2, E3 and E4… Expand
2010
2010
Background:Lung squamous cell carcinomas (SqCCs) occur at higher rates following arsenic exposure. Somatic DNA copy-number… Expand
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2010
2010
BACKGROUND The bladder exstrophy-epispadias complex (BEEC) is a spectrum of anomalies involving the abdominal wall, pelvis… Expand
Highly Cited
2009
Highly Cited
2009
To determine the pattern of genetic alterations in primary central nervous system lymphomas (PCNSL), 19 PCNSL were studied by… Expand
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Highly Cited
2006
Highly Cited
2006
The site-specific integrase from bacteriophage phiC31 functions in mammalian cells and is being applied for genetic engineering… Expand
2006
2006
BACKGROUND:  PRV‐1 mRNA is overexpressed by neutrophils from polycythemia vera patients and is homologous to NB1 a gene… Expand
Highly Cited
2006
Highly Cited
2006
Reports on insertional mutagenesis due to integration of gene therapy vectors into the host genome have raised concerns about the… Expand
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2005
2005
Lipid levels in plasma strongly influence the risk for coronary heart disease. To localise and subsequently identify genes… Expand
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