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5p15.33

A chromosome band present on 5p
National Institutes of Health

Related topics

Related topics

4 relations
Chromosome 5 Short ArmChromosomesTERT wt AlleleTRIP13 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Application of high‐resolution array platform for genome‐wide copy number variation analysis in patients with nonsyndromic cleft lip and palate
Although more than 14 loci may be involved in the development of nonsyndromic cleft lip and palate (NSCLP), the etiology has not… 
2017
2017
An evaluation study of reported pancreatic adenocarcinoma risk-associated SNPs from genome-wide association studies in Chinese population.
2016
2016
Genetic linkage studies of a North Carolina macular dystrophy family.
2015
2015
Lung Cancer Risk, Genetic Variation, and Air Pollution
2014
2014
Validation of association of genetic variants at 10q with prostate‐specific antigen (PSA) levels in men at high risk for prostate cancer
To validate six previously identified markers among men at increased risk of prostate cancer (African‐American men and those with… 
2012
2012
40 Mb duplication in chromosome band 5p13.1p15.33 with 800 kb terminal deletion in a foetus with mild phenotypic features.
2012
2012
Common genetic variants in TERT contribute to risk of cervical cancer in a Chinese population
Single‐nucleotide polymorphisms (SNPs) of TERT rs2736098, rs2736100, and CLPTM1L rs402710 at 5p15.33 are significantly associated… 
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… 
2010
2010
Genetic variations in TERT-CLPTM1L genes and risk of squamous cell carcinoma of the head and neck.
Single-nucleotide polymorphisms (SNPs) of TERT-rs2736098 (C > T) and CLPTM1L-rs401681(C > T) at the 5p15.33 locus are… 
2006
2006
A novel primate specific gene, CEI, is located in the homeobox gene IRXA2 promoter in Homo sapiens.
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