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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

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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… 
2011
2011
Genome wide profiling of tongue and cheek cancer using high resolution array based CGH
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… 
2007
2007
Comparative mapping of sheep chromosome 2q
Sheep chromosome 2q (OAR2q), which is homologous with human chromosome 2q (HSA2q), and cattle chromosome 2 (BTA2), is known to… 
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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