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13q12

A chromosome band present on 13q
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
To identify genetic susceptibility loci for nasopharyngeal carcinoma (NPC), a genome-wide association study was performed using… Expand
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Highly Cited
2005
Highly Cited
2005
Hearing impairment is a common and highly heterogeneous sensory disorder. Genetic causes are thought to be responsible for more… Expand
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Highly Cited
2003
Highly Cited
2003
The purpose of this study was to assess 65 pedigrees ascertained through a Bipolar I (BPI) proband for evidence of linkage, using… Expand
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Highly Cited
2002
Highly Cited
2002
BACKGROUND Inherited hearing impairment affects about 1 in 2000 newborns. Up to 50 percent of all patients with autosomal… Expand
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Highly Cited
1999
Highly Cited
1999
factors1. Mutations in the connexin26 gene (GJB2), located on 13q12, are responsible for non-syndromic recessive and dominant… Expand
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Highly Cited
1998
Highly Cited
1998
Inactivation of the klotho (kl) gene in mice results in multiple disorders that resemble human aging. The mouse kl gene encodes a… Expand
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Highly Cited
1998
Highly Cited
1998
Mutations in the Cx26 gene have been shown to cause autosomal recessive nonsyndromic hearing loss (ARNSHL) at the DFNB1 locus on… Expand
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Highly Cited
1994
Highly Cited
1994
Chromosome studies of lipomas have revealed an extensive cytogenetic heterogeneity. To investigate the frequencies of previously… Expand
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Highly Cited
1994
Highly Cited
1994
Non–syndromic, recessively inherited deafness is the most predominant form of severe inherited childhood deafness. Until now, no… Expand
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Review
1993
Review
1993
Research in oncogenetics has led to the identification of two major classes of tumor‐associated genes, oncogenes and tumor… Expand
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