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20q13.33

A chromosome band present on 20q
National Institutes of Health

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7 relations
20qChromosomesGATA5 wt AlleleMIR1-1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Whole exome-wide association study identifies a missense variant in SLC2A4RG associated with glioblastoma risk.
In this study, we conducted a genome-wide scan of single nucleotide polymorphisms (SNPs) to identify coding variants that is… 
Review
2013
Review
2013
Qualitative and quantitative expression status of the human chromosome 20 genes in cancer tissues and the representative cell lines.
Under the guidance of the Chromosome-centric Human Proteome Project (C-HPP), (1, 2) we conducted a systematic survey of the… 
2013
2013
Additional evidence to support the role of the 20q13.33 region in susceptibility to autism
Additional Evidence to Support the Role of the 20q13.33 Region in Susceptibility to Autism Anne-Laure Mosca-Boidron,* Myl ene… 
2012
2012
Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients.
Recent genome-wide association studies have identified single-nucleotide polymorphisms at 16 genetic loci associated with… 
2012
2012
PSMA7 inhibits the tumorigenicity of A549 human lung adenocarcinoma cells
The gene for proteasome subunit alpha type-7 (PSMA7) is located in chromosomal 20q13.33, a region frequently amplified in tumor… 
2012
2012
Association Analysis of Single Nucleotide Polymorphisms at Five Loci: Comparison between Atopic Dermatitis and Asthma in the Chinese Han Population
Atopic diseases, such as atopic dermatitis (AD) and asthma, are closely related to clinical phenotypes with hypersensitivity, and… 
2012
2012
Genetic variant rs4982958 at 14q11.2 is associated with allergic rhinitis in a Chinese Han population running title: 14q11.2 is a susceptibility locus for allergic rhinitis.
BACKGROUND Allergic rhinitis (AR) is one of the most common diseases caused by the combined effects of intrinsic factors… 
2011
2011
De Novo Deletion of Chromosome 20q13.33 in a Patient with Tracheo-esophageal Fistula, Cardiac Defects and Genitourinary Anomalies Implicates GTPBP5 as a Candidate Gene
BACKGROUND Tracheo-esophageal fistula (TEF) with/or without esophageal atresia (EA) is a common congenital malformation that is… 
Highly Cited
2010
Highly Cited
2010
Interaction between 5 genetic variants and allergy in glioma risk.
The etiology of glioma is barely known. Epidemiologic studies have provided evidence for an inverse relation between glioma risk… 
Review
2007
Review
2007
A de novo 1.1–1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features
We report on a de novo submicroscopic deletion of 20q13.33 identified by subtelomeric fluorescence in situ hybridization (FISH… 
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