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2q21.1

A chromosome band present on 2q
National Institutes of Health

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2 relations
CFC1 wt AlleleChromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Admixture mapping of uterine fibroid size and number in African American women.
2015
2015
Duplication and deletion of CFC1 associated with heterotaxy syndrome.
Heterotaxy syndrome, which causes significant morbidity and mortality, is a class of congenital disorders, in which normal left… 
2014
2014
Recurrent microdeletion 2q21.1: Report on a new patient with neurological disorders
Whole genome profiling such as array comparative genomic hybridization has identified novel genomic imbalances. Copy number… 
2012
2012
Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148.
We have identified a rare small (~450 kb unique sequence) recurrent deletion in a previously linked attention-deficit… 
2012
2012
Analysis of molecular cytogenetic alterations in uterine leiomyosarcoma by array-based comparative genomic hybridization
ObjectiveThe aim of this study was to identify novel genes following genomic DNA copy number changes using a genome-wide array… 
2010
2010
AMY2A: a possible tumor-suppressor gene of 1p21.1 loss in gastric carcinoma.
Homozygous deletions (HDs) are major genomic forces contributing to the development of many solid tumors. To identify critical… 
2008
2008
Where do we go for atherothrombotic disease genetics?
See related articles, pages 1109–1120. Cardiovascular disease (CVD), including coronary artery disease (CAD) with its fatal… 
Highly Cited
2000
Highly Cited
2000
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.
Coronary heart disease (CHD) is a complex disorder constituting a major health problem in Western societies. To assess the… 
1997
1997
Genomic structure and chromosomal localization of the gene encoding translin, a recombination hotspot binding protein.
Human Translin is a novel DNA end binding protein that specifically recognizes consensus sequences at the breakpoint junctions in… 
1992
1992
De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies
SummaryA de novo and apparently balanced complex chromosome rearrangement (CCR) was found in monozygotic (MZ) twin infants with… 
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