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14q13.3

Part of the chromosome bands present on the long (q) arm of chromosome 14.
National Institutes of Health

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4 relations
CTAGE5 wt AlleleChromosomesNKX2-8 wt Allelechromosome 14q

Papers overview

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2018
2018
Child Neurology: Siblings with infantile epilepsy and developmental delay
Objective Chromosome 14q11-q22 deletion syndrome (OMIM 613457) is a rare genomic disorder with a variable phenotype. Methods We… 
2017
2017
Age at diagnosis and gender modify the risk of 9q22 and 14q13 polymorphisms for papillary thyroid carcinoma.
INTRODUCTION Papillary thyroid cancer (PTC) shows familial occurrence, and some susceptibility single nucleotide polymorphisms… 
Review
2015
Review
2015
Genetic Predisposition for Nonmedullary Thyroid Cancer
Nonmedullary thyroid cancer (NMTC) can be sporadic or can occur as a component cancer as part of several well-described… 
2014
2014
Are the SNPs of NKX2-1 associated with papillary thyroid carcinoma in the Han population of Northern China?
Papillary thyroid carcinoma (PTC) is one of the most common tumors of the thyroid gland. The common risk factors of PTC include… 
2013
2013
Concurrent overexpression of RET/PTC1 and TTF1 confers tumorigenicity to thyrocytes
A variant located on 14q13.3 nearest to thyroid transcription factor-1 (TTF1) predisposes individuals to thyroid cancer, but… 
2012
2012
Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial Synpolydactyly
Synpolydactyly is a relatively rare malformation. Recently, we came across a male infant with a familial synpolydactyly of the… 
2012
2012
Revision of “A 223-kb De Novo Deletion of PAX9 in a Patient With Oligodontia”
AbstractThe PAX (paired box) genes are a family of transcription factors critical for fetal growth and organogenesis… 
2010
2010
A 223-kb De Novo Deletion of PAX9 in a Patient With Oligodontia
The PAX (paired box) genes are a family of transcription factors critical for fetal growth and organogenesis. Abnormalities of… 
Highly Cited
2009
Highly Cited
2009
TTF1 expression in non‐small cell lung carcinoma: association with TTF1 gene amplification and improved survival
Acquired chromosomal aberrations play an important role in tumour development and progression. Such genetic alterations occur in… 
2008
2008
Use of co-activation of lung cancer specific developmental pathway genes, TTF-1, NKX2–8, and PAX9, to predict prognosis and guide therapeutic strategies
7511 Background: We recently described a novel, recurring amplicon (14q13.3) specific to NSCLC that harbors three genes, TTF- 1… 
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