14q21-q22

A chromosome band present on 14q
National Institutes of Health

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2006
2006
Glaucoma is a leading cause of vision impairment and blindness in both developed and developing countries. Primary open angle… Expand
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2001
2001
Editor—Recently, Reid et al 1 reported reduction of the chromosome 12q locus for autosomal dominant hereditary spastic paraplegia… Expand
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2000
2000
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss German kindred. DNA samples… Expand
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1998
1998
Mouse and rat genome studies are vital to the use of rodents as models of biology and human genetic disease. In this study… Expand
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1998
1998
This paper describes the cDNA cloning, genomic organization, and expression of the human RTN2 gene on chromosome 19q13.3, which… Expand
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1998
1998
Human DNA polymerase epsilon is composed of a 261 kDa catalytic polypeptide and a 55 kDa small subunit of unknown function. cDNAs… Expand
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1997
1997
Method of mapping: FISH and in situ hybridization Database depository information: GenBank J02921, M35368, M36682, M64303… Expand
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1995
1995
The two cDNA clones pHGCH1 and pHSR1, harboring partial coding sequences for GTPCH and SR, respectively, were tritium-labeled by… Expand
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1994
1994
We have determined the chromosomal localization of four human homeobox-containing genes, EMX1, EMX2, OTX1, and OTX2, related to… Expand
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