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7p21.3

A chromosome band present on 7p
National Institutes of Health

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AGR2 wt AlleleChromosome 7 Short ArmChromosomesRPA3 wt Allele

Papers overview

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2017
2017
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS)
To identify germ line variants contributing to the development of monoclonal gammopathy of undetermined significance (MGUS), an… 
2014
2014
Prenatal diagnosis of craniosynostosis (compound Saethre-Chotzen syndrome phenotype) caused by a de novo complex chromosomal rearrangement (1; 4; 7) with a microdeletion of 7p21.3-7p15.3, including…
Craniosynostosis (a premature fusion of the cranial sutures) occurs with a frequency of 1 in 2100-2500 births and in over 40… 
2013
2013
Genome‐wide linkage scan in affected sibling pairs identifies novel susceptibility region for venous thromboembolism: Genetics In Familial Thrombosis study
Venous thromboembolism (VTE) is a multicausal disorder involving environmental and genetic risk factors. In many thrombophilic… 
2012
2012
Association between copy number variants in 16p11.2 and major depressive disorder in a German case–control sample
The majority of genetic risk factors for major depressive disorder (MDD) still await identification. Since copy number variants… 
Highly Cited
2011
Highly Cited
2011
Copy Number Variants in Extended Autism Spectrum Disorder Families Reveal Candidates Potentially Involved in Autism Risk
Copy number variations (CNVs) are a major cause of genetic disruption in the human genome with far more nucleotides being altered… 
2010
2010
Short communication Characterization of FRA7B, a human common fragile site mapped at the 7p chromosome terminal region
Common fragile sites (CFS) are specific regions of the mammalian chromosomes that are particu- larly prone to gaps and breaks… 
2008
2008
TWIST microdeletion identified by array CGH in a patient presenting Saethre-Chotzen phenotype and a complex rearrangement involving chromosomes 2 and 7.
2007
2007
Establishment and characterization of a new xenograft-derived human esophageal squamous cell carcinoma cell line HKESC-4 of Chinese origin.
Highly Cited
2006
Highly Cited
2006
Evaluation of AGR2 and AGR3 as candidate genes for inflammatory bowel disease
Linkage analyses have implicated chromosome 7p21.3 as a susceptibility region for inflammatory bowel disease (IBD). Recently, the… 
2000
2000
Localization1 of the human anterior gradient-2 gene (AGR2) to chromosome band 7p21.3 by radiation hybrid mapping and fluorescencein situ hybridisation
Kuang et al. (1998) isolated 29 gene fragments that were coexpressed with ER (estrogen receptor) in breast carcinoma cell lines… 
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