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21q21.2

A chromosome band present on 21q
National Institutes of Health

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5 relations
21qADAMTS1 wt AlleleCD160 wt AlleleCKS1B wt Allele

Papers overview

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2018
2018
Möbius syndrome with cardiac rhabdomyomas
ABSTRACT Background: Möbius syndrome is a rare congenital condition which presents not merely with 6th and 7th nerve palsies, but… 
2015
2015
A Genome-Wide Association Study of Intraocular Pressure in Latinos
Intraocular pressure (IOP) is a major, as well as the only modifiable, risk factor for glaucoma. With an expected increase in the… 
2012
2012
Pure duplication 21q21.2-->qter due to a rea(21) in a Down syndrome girl. Remarks on nomenclature.
We report on an 8-year-old girl with a typical Down syndrome phenotype and a 46,XX,rea(21)(qter-->p12::q21.2-->qter).ish rea(21… 
2007
2007
An innocuous duplication of 11.2 Mb at 13q21 is gene poor: Sub‐bands of gene paucity and pervasive CNV characterize the chromosome anomalies
A boy with autistic spectrum disorder without dysmorphisms was found to have a chromosome duplication of part of band 13q21. His… 
1997
1997
[The genetics of Alzheimer's disease.].
The aetiology of Alzheimer's disease (AD) is still unknown, but a small fraction of AD patients have a dominant inherited defect… 
1993
1993
The effect of Robertsonian translocation on recombination on chromosome 21.
To test the hypothesis that Robertsonian translocation may lead to altered crossing-over on both chromosomes involved in the… 
1992
1992
Isolation, characterization, and regional mapping of microclones from a human chromosome 21 microdissection library.
Thirty-four unique-sequence microclones were isolated from a previously described microdissection library of human chromosome 21… 
1989
1989
Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome
SummaryWe used a mouse-human somatic cell hybrid to construct a chromosome 21-enriched library in phage vector EMBL4. In all, 35… 
Highly Cited
1985
Highly Cited
1985
Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction.
A number of unique sequence recombinant DNA clones were isolated from a recombinant DNA library constructed from DNA enriched for… 
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