Chromosome 21 monosomy

Known as: Monosomy 21 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1997-2015
0119972015

Papers overview

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2016
2016
Monosomy 21 is an extremely rare genetic disorder presenting with a wide array of symptoms. Recurrent infections, some life… (More)
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2016
2016
IInterstitial 21q deletions can cause a wide spectrum of symptoms depending on the size and the location of the deletion. It has… (More)
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2015
2015
In this report, we describe a patient with azoospermia in conjection with de novo ring chromosome 21 and monosomy 21 mosaicism… (More)
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Review
1998
Review
1998
A case is presented in which monosomy 21 was detected by routine cytogenetics and fluorescence in situ hybridization (FISH… (More)
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1997
1997
We describe a case of full monosomy 21 which was prenatally diagnosed in chorionic villi by fluorescent in situ hybridization… (More)
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