Skip to search formSkip to main contentSkip to account menu

10q21.1

A chromosome band present on 10q
National Institutes of Health

Related topics

Related topics

5 relations
10qCDK1 wt AlleleCISD1 wt AlleleChromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma
Pituitary adenoma is one of the most common intracranial neoplasms, and its genetic basis remains largely unknown. To identify… 
2013
2013
Copy number variation findings among 50 children and adolescents with autism spectrum disorder
Objectives Autism spectrum disorders (ASDs) are a heterogeneous group of neurodevelopment disorders with a complex genetic… 
2007
2007
An innocuous duplication of 11.2 Mb at 13q21 is gene poor: Sub‐bands of gene paucity and pervasive CNV characterize the chromosome anomalies
A boy with autistic spectrum disorder without dysmorphisms was found to have a chromosome duplication of part of band 13q21. His… 
2007
2007
Dissecting the heterogeneity of rheumatoid arthritis through linkage analysis of quantitative traits.
OBJECTIVE To dissect the heterogeneity of rheumatoid arthritis (RA) through linkage analysis of quantitative traits, specifically… 
2006
2006
A genome‐wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba
We present results from a genome‐wide scan of a six generation pedigree with 28 affected members with apparently dominant bipolar… 
Highly Cited
2004
Highly Cited
2004
Possible association of mitochondrial transcription factor A (TFAM) genotype with sporadic Alzheimer disease
2002
2002
Loss of heterozygosity on chromosome 10q is associated with earlier onset sporadic colorectal adenocarcinoma
Recent studies have shown that loss of heterozygosity (LOH) on chromosome 10q is a frequent event in a number of tumour types… 
1994
1994
Divergent structure of the human synexin (annexin VII) gene and assignment to chromosome 10.
The human synexin (annexin VII) gene occurs as a single copy at chromosome 10q21.1-21.2 and substantially deviates in size and in… 
1992
1992
Complementary physical and genetic techniques map the vinculin (VCL) gene on chromosome 10q.
1987
1987
A polymorphic locus, D10S5, at 10q21.1
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)