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2q31.1

Part of the chromosome bands present on the long (q) arm of chromosome 2.
National Institutes of Health

Related topics

Related topics

9 relations
CHN1 wt AlleleChromosomesHOXD11 wt AlleleHOXD13 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.
OBJECTIVE Congenital cardiac defects represent the most common group of birth defects, affecting an estimated six per 1000 births… 
Review
2015
Review
2015
Selective chromatid segregation mechanism proposed for the human split hand/foot malformation development by chromosome 2 translocations: A perspective.
2013
2013
Diabetic nephropathy: is ESRD its only heritable phenotype?
Genetic susceptibility contributes to the overall risk of nephropathy among individuals with diabetes. In this issue of JASN… 
2013
2013
Chromosome 2 q 31 . 1 Associates with ESRD in Women with Type 1 Diabetes
Sex and genetic variation influence the risk of developing diabetic nephropathy and ESRD in patients with type 1 diabetes. We… 
2013
2013
Combined Genome-Wide Linkage and Association Analyses of Fasting Glucose Level in Healthy Twins and Families of Korea
This study was undertaken to identify genetic polymorphisms that are associated with the risk of an elevated fasting glucose (FG… 
2010
2010
A dominant mesomelic dysplasia associated with a 1.0-Mb microduplication of HOXD gene cluster at 2q31.1
A three-generation family with four patients affected by a novel mesomelic dysplasia was investigated for genome-wide DNA copy… 
2010
2010
Genome scan meta-analysis in systemic lupuserythematosus strong linkage with loci 6p22.3-p21.1and 2q31.1-34
The genetic contribution to development of system lupus erythematosus (SLE) is well established. Several genome scan studies have… 
2006
2006
Delineation of a 2q deletion in a girl with dysmorphic features and epilepsy
In recent years, the spectrum of available methods for the characterization of chromosomal aberrations has significantly… 
2005
2005
Suggestive evidence for association of D2S2188 marker (2q31.1) with autism in 143 Sicilian (Italian) TRIO families
We have screened 143 Sicilian (Italian) families with one autistic child to verify, by a linkage disequilibrium approach, the… 
2003
2003
An acceptor splice site mutation in HOXD13 results in variable hand, but consistent foot malformations
HOXD13 is the most 5′ of the HOXD cluster of homeobox genes in chromosome band 2q31.1. Heterozygous expansions of a polyalanine… 
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