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2q21.3

A chromosome band present on 2q.
National Institutes of Health

Topic mentions per year

Topic mentions per year

1987-2016
01219872016

Related topics

Related topics

3 relations
ChromosomesMIR128-1 wt AlleleZRANB3 wt Allele

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
2q21.3
Chromosomes
ZRANB3 wt Allele
MIR128-1 wt Allele

Papers overview

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2017
2017
[Delineating a case with a complex karyotype by using combined genetic techniques].
OBJECTIVE To explore the pathogenesis of a child with growth retardation, liver damage and congenital heart disease. METHODS G… (More)
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2016
Review
2016
Genetics in Keratoconus: where are we?
Keratoconus (KC) is a non-inflammatory thinning and protrusion of the cornea in which the cornea assumes a conical shape. Complex… (More)
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2013
2013
Angelman syndrome and severe infections in a patient with de novo 15q11.2-q13.1 deletion and maternally inherited 2q21.3 microdeletion.
Angelman syndrome is a neurodevelopmental disorder characterized by mental retardation, severe speech disorder, facial… (More)
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2013
2013
[Anaplastic large cell lymphoma: an array-based comparative genomic hybridization study].
OBJECTIVE To use array-based comparative genomic hybridization (aCGH) technology to study the molecular cytogenetic abnormalities… (More)
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2012
2012
A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.
Keratoconus is a condition in which the cornea progressively thins over time, and is a major cause for cornea transplantation. To… (More)
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2012
2012
Use of germline polymorphisms in predicting concurrent chemoradiotherapy response in esophageal cancer.
PURPOSE To identify germline polymorphisms to predict concurrent chemoradiation therapy (CCRT) response in esophageal cancer… (More)
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2008
2008
A single nucleotide polymorphism at chromosome 2q21.3 (LCT -13910C>T) associates with clinical outcome after allogeneic hematopoietic stem cell transplantation.
A single nucleotide polymorphism (SNP) responsible for lactase persistence (LCT -13910C>T) changes intestinal microflora… (More)
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2006
Review
2006
Prenatal diagnosis of de novo interstitial 2q14.2-2q21.3 deletion assisted by array-based comparative genomic hybridization: a case report.
BACKGROUND During conventional karyotyping, it can be difficult to clearly identify de novo interstitial deletion of a… (More)
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1987
1987
Chromosome studies in inherited nonpolyposis colon cancer syndrome.
This study was designed to determine if any constitutional chromosomal markers were linked with the expression of colorectal… (More)
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