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14q31

A chromosome band present on 14q
National Institutes of Health

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ChromosomesGPR68 wt AlleleTSHR wt Allelechromosome 14q

Papers overview

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2007
2007
Linkage of Graves’ disease to the human leucocyte antigen region in the Chinese‐Han population in Taiwan
Objective  To investigate whether markers in the candidate chromosome regions, including the human leucocyte antigen (HLA) region… 
2006
2006
Identification of a 7.1-mega base pairs minimal deletion at 14q31.1-32.11 in adenocarcinomas of the gastroesophageal junction.
2003
2003
Further indications for genetic heterogeneity of euthyroid familial goiter
Iodine deficiency is the most important etiological factor for euthyroid endemic goiter. However, family and twin pair studies… 
2001
2001
Maternally inherited duplication of the possible imprinted 14q31 region
The existence of parent of origin differences in the expression of some genes, a process known as genomic imprinting, has been… 
1999
1999
Assignment1 of fibulin-5 (FBLN5) to human chromosome 14q31 by in situ hybridization and radiation hybrid mapping
We recently reported the cloning and expression pattern of the rat embryonic vascular EGF repeat-containing (EVEC) cDNA (Kowal et… 
Review
1999
Review
1999
Interstitial Deletion of 14q, 46, XY, del (14) (q24.3q32.1) Associated With Status Nonepileptic Myoclonia and Delayed Myelination
A Japanese boy with interstitial deletion of the long arm of chromosome 14, including band 14q31, is described. The… 
1998
1998
NEW SONOGRAPHIC FINDINGS IN A FETUS WITH AN INTERSTITIAL DELETION IN THE LONG ARM OF CHROMOSOME 14
1995
1995
Molecular analysis of three patients with interstitial deletions of chromosome band 14q31.
Two patients and one three generation family with interstitial deletions of distal chromosome band 14q31 are described. The… 
1993
1993
The human cytochrome b5 gene and two of its pseudogenes are located on chromosomes 18q23, 14q31-32.1 and 20p11.2, respectively
Using very high stringency hybridization conditions for the Southern blot hybridization analysis of hamster-human cell hybrid DNA… 
1992
1992
Deletion (14) (q24.3q32.1): evidence for a distinct clinical phenotype.
We report on a 4-year-old girl with distinctive facial features (redundant skin, bushy eyebrows, narrow palpebral fissures, short… 
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