15q26.3

A chromosome band present on 15q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1993-2017
02419932017

Papers overview

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2016
2016
Terminal duplications of 15q26.3 are associated with an overgrowth phenotype, distinct facial features and intellectual… (More)
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2013
2013
Autosomal recessive congenital ichthyosis (ARCI) is a rare genetic disorder of the skin characterized by abnormal desquamation… (More)
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2012
2012
Central corneal thickness (CCT) is a highly heritable trait. Genes that significantly influence CCT can be candidate genes for… (More)
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2011
2011
BACKGROUND Presence of left ventricular hypertrophy on an ECG (ECG-LVH) is widely assessed clinically and provides prognostic… (More)
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2010
2010
The maternal and paternal genomes possess distinct epigenetic marks that distinguish them at imprinted loci. In order to identify… (More)
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Highly Cited
2007
Highly Cited
2007
The Family Investigation of Nephropathy and Diabetes (FIND) was initiated to map genes underlying susceptibility to diabetic… (More)
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2006
2006
Most Wilms' tumors are of low stage, favorable histology, and have a high likelihood of cure with current multimodal therapy… (More)
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2001
2001
Desmuslin is an α-dystrobrevin-interacting protein expressed primarily in heart and skeletal muscle. The desmuslin protein… (More)
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2001
2001
Intermediate filament (IF) proteins are constituents of the cytoskeleton, conferring resistance to mechanical stress, and are… (More)
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1993
1993
An 11-year-old girl with de novo r(15) (p12q26.3) with a clinical diagnosis of Silver-Russell syndrome (SRS) is presented. She… (More)
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