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13q12

A chromosome band present on 13q
National Institutes of Health

Papers overview

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Review
2010
Review
2010
Highly Cited
2010
Highly Cited
2010
To identify genetic susceptibility loci for nasopharyngeal carcinoma (NPC), a genome-wide association study was performed using… 
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… 
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… 
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… 
Highly Cited
1999
Highly Cited
1999
factors1. Mutations in the connexin26 gene (GJB2), located on 13q12, are responsible for non-syndromic recessive and dominant… 
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… 
Review
1993
Review
1993
Research in oncogenetics has led to the identification of two major classes of tumor‐associated genes, oncogenes and tumor… 
Highly Cited
1978
Highly Cited
1978
SUMMARY: A new syndrome of autosomal recessive spastic ataxia has been isolated in the Charlevoix-Saguenay region of Quebec. This…