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15q26.3

A chromosome band present on 15q
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2012
Highly Cited
2012
Central corneal thickness (CCT) is a highly heritable trait. Genes that significantly influence CCT can be candidate genes for… Expand
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Highly Cited
2011
Highly Cited
2011
Preterm birth is the major cause of neonatal death and serious morbidity. Most preterm births are due to spontaneous onset of… Expand
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Highly Cited
2009
Highly Cited
2009
Background Silver–Russell syndrome (SRS, OMIM 180860) features fetal and postnatal growth restriction and variable dysmorphisms… Expand
2009
2009
Background IGF1R (insulin-like growth factor 1 receptor) haploinsufficiency is a rare event causing difficulties in defining… Expand
Highly Cited
2007
Highly Cited
2007
The Family Investigation of Nephropathy and Diabetes (FIND) was initiated to map genes underlying susceptibility to diabetic… Expand
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2006
2006
Leucine-rich repeat kinase 1 gene (LRRK1) on chromosome 15q26.3 is a paralog of LRRK2 in which multiple substitutions were… Expand
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Review
2005
Review
2005
  • Q. Wang
  • Current atherosclerosis reports
  • 2005
  • Corpus ID: 40330894
Exciting advances have been made recently in genetic studies of coronary artery disease (CAD), myocardial infarction (MI), and… Expand
Highly Cited
2001
Highly Cited
2001
Intermediate filament (IF) proteins are constituents of the cytoskeleton, conferring resistance to mechanical stress, and are… Expand
2001
2001
BackgroundDesmuslin is an α-dystrobrevin-interacting protein expressed primarily in heart and skeletal muscle. The desmuslin… Expand
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Highly Cited
1993
Highly Cited
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… Expand