Non-Trisomic Autosomal Aneuploidy

Known as: Aneuploid Chromosome Number - Non-Trisomic 
Autosomal aneuploidy not associated with trisomy. It results in developmental malformations.
National Institutes of Health

Topic mentions per year

Topic mentions per year

1970-2017
0119702017

Papers overview

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Review
2017
Review
2017
Overexpression of Dual-specificity tyrosine-phosphorylated regulated kinase 1A (DYRK1A), located on human chromosome 21, may… (More)
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Review
2016
Review
2016
The distinction between partial hydatidiform mole (PHM) and trisomy gestation is not always straightforward histologically and it… (More)
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2015
2015
Trisomy 21 causes skeletal alterations in individuals with Down syndrome (DS), but the causative trisomic gene and a therapeutic… (More)
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2002
2002
We have assessed the effects of enriched environment (EE) upon behavioral and cognitive performances of partially trisomic Ts65Dn… (More)
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1997
1997
Our aim was to investigate the contribution of certain antenatally detectable markers leading to the diagnosis of trisomic… (More)
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Review
1996
Review
1996
We report on a fetus with 47,XX,+15 chromosome abnormality detected on chorionic villus sampling (CVS). The pregnancy was… (More)
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Review
1996
Review
1996
Data on human trisomic conceptuses suggest that the extra chromosome commonly has a maternal origin, and the amount and position… (More)
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Review
1995
Review
1995
Aneuploidy is the most common class of chromosome abnormality in humans, occurring in at least 0.3% of newborns and approximately… (More)
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1990
1990
Karyotypes were analyzed using directing method for chorionic villi chromosome preparation in 52 specimens from spontaneous… (More)
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1970
1970
Recently developed pachytene maps of the two small acrocentric autosomes (numbers 21 and 22) of man have been applied to a case… (More)
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