15q21

A chromosome band present on 15q
National Institutes of Health

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Highly Cited
2008
Highly Cited
2008
A genome-wide association study was performed to identify genetic factors involved in susceptibility to psoriasis (PS) and… (More)
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Highly Cited
2004
Highly Cited
2004
Dyslexia has been linked to a number of chromosomal regions including 15q. Recently a gene, EKN1, with unknown function in the… (More)
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Highly Cited
2004
Highly Cited
2004
To examine the genetic basis of age-related macular degeneration (ARMD), a degenerative disease of the retinal pigment epithelium… (More)
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Highly Cited
2003
Highly Cited
2003
Approximately 3-10% of people have specific difficulties in reading, despite adequate intelligence, education, and social… (More)
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2001
2001
Congenital cataract is a clinically and genetically highly heterogeneous eye disorder, with autosomal dominant inheritance being… (More)
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Highly Cited
2000
Highly Cited
2000
Griscelli syndrome (GS, MIM 214450), a rare, autosomal recessive disorder, results in pigmentary dilution of the skin and the… (More)
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2000
2000
Griscelli syndrome is a rare autosomal recessive disease characterized by pigment dilution, variable cellular immunodeficiency… (More)
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Highly Cited
1997
Highly Cited
1997
Griscelli disease (OMIM 214450) is a rare autosomal recessive disorder characterized by pigmentary dilution, variable cellular… (More)
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1997
1997
The childhood neuronal ceroid lipofuscinoses (NCLs) are a group of autosomal recessive neurodegenerative disorders characterised… (More)
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Highly Cited
1987
Highly Cited
1987
We have used cDNA probes for lipoprotein lipase and hepatic lipase to determine the chromosomal and subchromosomal locations of… (More)
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