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15q26.3

A chromosome band present on 15q
National Institutes of Health

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Highly Cited
2013
Highly Cited
2013
The following information was missing from the Funding section: "This work has been supported in part by grants to M. Lathrop… Expand
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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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2011
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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2009
2009
BACKGROUND Silver-Russell syndrome (SRS, OMIM 180860) features fetal and postnatal growth restriction and variable dysmorphisms… Expand
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2009
2009
BACKGROUND IGF1R (insulin-like growth factor 1 receptor) haploinsufficiency is a rare event causing difficulties in defining… Expand
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2008
2008
We tried to establish models that predict systemic recurrence in breast cancer by selecting marker clones with DNA copy number… Expand
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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… 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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2001
2001
Intermediate filament (IF) proteins are constituents of the cytoskeleton, conferring resistance to mechanical stress, and are… Expand
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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… Expand
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