Chromosome 13q trisomy

Known as: 13q syndrome, Duplication 13q, Trisomy 13q 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1976-2016
012319762016

Papers overview

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2016
2016
Two infants with retinoblastoma and 13q syndrome with multiorgan system anomalies were treated with targeted intra-arterial… (More)
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2014
2014
Patients with 13q deletion syndrome are characterized with different phenotypical features depending on the size and location of… (More)
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Review
2014
Review
2014
Ion channels are crucial components of cellular excitability and are involved in many neurological diseases. This review focuses… (More)
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2014
2014
We report a 12-year-old boy referred to the Clinical Genetics service in view of facial dysmorphism, learning difficulties and… (More)
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2011
2011
INTRODUCTION The co-occurrence of ring chromosome 13 syndrome and 47, XYY syndrome in the same individual is rare. To the best of… (More)
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2011
2011
Large numbers of patients with deletions of the long arm of chromosome 13 have been described. However, only a few instances have… (More)
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2007
2007
The phenotypic description of deletion 13q syndrome is dependent on the location and size of the deleted segment. At present, the… (More)
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2006
2006
Context: The deletion of the short arm of the chromosome 13, also known as 13q syndrome, is an extremely rare chromosomal… (More)
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Review
2005
Review
2005
Two cases of newborns with deletion 13q syndrome were identified and studied using electron microscopy and histologic… (More)
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