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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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Review
2010
Review
2010
Mutations within the FMS-like tyrosine kinase 3 (FLT3) gene on chromosome 13q12 have been detected in up to 35% of acute myeloid… 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
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
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
Highly Cited
1994
Highly Cited
1994
Chromosome studies of lipomas have revealed an extensive cytogenetic heterogeneity. To investigate the frequencies of previously… Expand
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
Review
1993
Review
1993
Research in oncogenetics has led to the identification of two major classes of tumor‐associated genes, oncogenes and tumor… Expand