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2q21.3

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

Related topics

Related topics

3 relations
ChromosomesMIR128-1 wt AlleleZRANB3 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Lactase Persistence in Southern Iberia and Northwestern Africa: New Insights into the Population Structure and History of Western Mediterranean
The development of lactose tolerance in humans represents a fair example of interaction between biology and culture. Lactase… Expand
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Review
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… Expand
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2015
2015
SnapShot: Genetics of Parkinson’s Disease
Different types of genetic technologies and approaches allow for the study and identification of different types of genetic… Expand
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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… Expand
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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… Expand
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Highly Cited
2012
Highly Cited
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… Expand
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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… Expand
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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… Expand
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Review
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… Expand
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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… Expand
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