FAQ

19q13.31

A chromosome band present on 19q
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2017
012320042017

Related topics

Related topics

2 relations
19qChromosomes

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
19q13.31
Chromosomes
19q

Papers overview

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2015
2015
Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
STUDY QUESTION Can the use of whole-exome sequencing (WES) together with single nucleotide polymorphism (SNP) array help to… (More)
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2012
2012
Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients
BACKGROUND Specific genetic contributions for preeclampsia (PE) are currently unknown. This genome-wide association study (GWAS… (More)
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2010
2010
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family.
BACKGROUND The bladder exstrophy-epispadias complex (BEEC) is a spectrum of anomalies involving the abdominal wall, pelvis… (More)
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2009
2009
Chromosomal imbalances and partial uniparental disomies in primary central nervous system lymphoma
To determine the pattern of genetic alterations in primary central nervous system lymphomas (PCNSL), 19 PCNSL were studied by… (More)
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Highly Cited
2006
Highly Cited
2006
Integration specificity of phage phiC31 integrase in the human genome.
The site-specific integrase from bacteriophage phiC31 functions in mammalian cells and is being applied for genetic engineering… (More)
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2006
2006
The gene overexpressed in polycythemia rubra vera, PRV-1, and the gene encoding a neutrophil alloantigen, NB1, are alleles of a single gene, CD177, in chromosome band 19q13.31.
BACKGROUND PRV-1 mRNA is overexpressed by neutrophils from polycythemia vera patients and is homologous to NB1 a gene… (More)
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2006
2006
Molecular analysis of chromosomal rearrangements in mammalian cells after phiC31-mediated integration.
Reports on insertional mutagenesis due to integration of gene therapy vectors into the host genome have raised concerns about the… (More)
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2005
2005
Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions
Lipid levels in plasma strongly influence the risk for coronary heart disease. To localise and subsequently identify genes… (More)
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2005
2005
Genome-wide analyses demonstrate novel loci that predispose to drusen formation.
PURPOSE To test whether genes for drusen formation are independent of age-related macular degeneration (AMD) pathogenesis… (More)
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2004
2004
Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q
Platelet count is a highly heritable trait with genetic factors responsible for around 80% of the phenotypic variance. We… (More)
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