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18q21.31

A chromosome band present on 18q
National Institutes of Health

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4 relations
ALPK2 wt AlleleChromosomesMIR122 wt Allelechromosome 18q

Papers overview

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2015
2015
Deletion of the MC4R gene in a 9-year-old obese boy.
BACKGROUND The most common monogenic form of obesity is caused by mutations in the melanocortin 4 receptor (MC4R) gene. More than… 
2012
2012
Loss of heterozygosity at chromosomes 1p35-pter, 4q, and 18q and protein expression differences between adenocarcinomas of the distal stomach and gastric cardia.
2012
2012
Abnormal Myelination in Ring Chromosome 18 Syndrome
Partial deletion of genetic material from the long arm of chromosome 18 results in a syndrome with multisystemic involvement… 
2011
2011
Search for inherited susceptibility to radiation-associated meningioma by genomewide SNP linkage disequilibrium mapping
Background:Exposure to ionising radiation is a well-established risk factor for multiple types of tumours, including malignant… 
2009
2009
DNA fingerprinting tags novel altered chromosomal regions and identifies the involvement of SOX5 in the progression of prostate cancer
Identification of genomic alterations associated with the progression of prostate cancer may facilitate the better understanding… 
Highly Cited
2007
Highly Cited
2007
Genotype–phenotype mapping of chromosome 18q deletions by high‐resolution array CGH: An update of the phenotypic map
Partial deletions of the long arm of chromosome 18 lead to variable phenotypes. Common clinical features include a characteristic… 
Review
2007
Review
2007
Duplication 18q21.31‐q22.2
We report on three siblings with mild mental retardation and minor dysmorphic features carrying an interstitial duplication of… 
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… 
1999
1999
Fractional allele loss indicates distinct genetic populations in the development of squamous cell carcinoma of the head and neck (SCCHN).
Loss of heterozygosity (LOH) had been widely used to assess genetic instability in tumours and a high LOH on chromosome arms 3p… 
1985
1985
Thymidylate synthase-deficient Chinese hamster cells: a selection system for human chromosome 18 and experimental system for the study of thymidylate synthase regulation and fragile X expression.
Chinese hamster lung (CHL) V79 cells already deficient in hypoxanthine phosphoribosyltransferase were exposed to uv light and… 
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