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13q14-q21

A chromosome band present on 13q
National Institutes of Health

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3 relations
13qChromosomesHTR2A wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2014
Review
2014
Wilson's disease: neurological and psychiatric manifestations.
  • Arif Dalvi
  • Disease-a-month : DM
  • 2014
  • Corpus ID: 41853088
Review
2014
Review
2014
Is there a Link Between Anxiety , Depressive Disorders and 5 HT 2 A Receptor Gene Polymorphism ? – Study from A Conflict Area , India-controlled Kashmir
BACKGROUND: 5 HT-2A receptor gene polymorphisms are associated with various psychiatric disorders, including anxiety and… 
Review
2010
Review
2010
Does Serotonin 2A Receptor Gene Polymorphism Increase The Vulnerability To Panic Attacks
Many studies have been conducted to show the genetic associations between the serotonin 2A receptor (HTR2A) gene polymorphisms… 
Highly Cited
2000
Highly Cited
2000
The RB1 gene is the target of chromosome 13 deletions in malignant fibrous histiocytoma.
Forty-four malignant fibrous histiocytomas (MFHs) were studied by comparative genomic hybridization. Among the observed… 
2000
2000
[Application of the fluorescent in situ hybridization on the prenatal diagnosis of the fetal aneuploidy in the uncultured amniocytes].
OBJECTIVE To study the method and value of fluorescent in situ hybridization (FISH) on the rapid prenatal diagnosis of the fetal… 
1997
1997
Ultra-sensitive FISH is a useful tool for studying chronic HIV-1 infection.
1994
1994
MOLECULAR DIAGNOSIS OF PRESYMPTOMATIC Wilson's Disease
Wilson's disease (WND) is an autosomal recessive disorder of copper metabolism, The metabolic defect is still unknown, but the… 
1993
1993
Mapping of aldose reductase gene sequences to human chromosomes 1, 3, 7, 9, 11, and 13.
Aldose reductase (alditol:NAD(P)+ 1-oxidoreductase; EC 1.1.1.21) (AR) catalyzes the reduction of several aldehydes, including… 
1992
1992
Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene
SummaryWilson disease (WD) is an autosomal recessive disorder of copper metabolism. A minimum recombinant analysis using D13S22… 
Highly Cited
1991
Highly Cited
1991
Assignment of a serotonin 5HT-2 receptor gene (HTR2) to human chromosome 13q14-q21 and mouse chromosome 14.
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