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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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Highly Cited
2015
Highly Cited
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
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
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
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
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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