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5p13.3

A chromosome band present on 5p
National Institutes of Health

Related topics

Related topics

5 relations
Chromosome 5 Short ArmChromosomesGOLPH3 wt AlleleRNASEN wt Allele

Papers overview

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2016
2016
Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis
Because of genetic heterogeneity present in idiopathic scoliosis, we previously defined clinical subsets (a priori) from a sample… 
2014
2014
Structural Genomic Variation as Risk Factor for Idiopathic Recurrent Miscarriage
Recurrent miscarriage (RM) is a multifactorial disorder with acknowledged genetic heritability that affects ∼3% of couples aiming… 
2014
2014
Novel genetic aberrations in breast phyllodes tumours: comparison between prognostically distinct groups
Phyllodes tumours of the breast are uncommon fibroepithelial neoplasms which pose management challenges due to difficulties in… 
2013
2013
Molecular signatures of basal cell carcinoma susceptibility and pathogenesis: a genomic approach.
Gene expression profiling can be useful for phenotypic classification, investigation of functional pathways, and to facilitate… 
Review
2012
Review
2012
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity
Purpose:A small supernumerary marker chromosome is often seen in patients with developmental disorders. Prior to array-based… 
2011
2011
Transmitted deletions of medial 5p and learning difficulties; Does the cadherin cluster only become penetrant when flanking genes are deleted?
The central portion of the short arm of chromosome 5 is unusual in that large, cytogenetically visible interstitial deletions… 
2007
2007
Gain and overexpression of the oncostatin M receptor occur frequently in cervical squamous cell carcinoma and are associated with adverse clinical outcome
For many oncogenes, increased expression resulting from copy number gain confers a selective advantage to cells that consequently… 
2002
2002
A genome-wide linkage scan for steroids and SHBG levels in black and white families: the HERITAGE Family Study.
To identify loci-harboring genes affecting steroid hormone and SHBG plasma levels, a genomic-wide scan was performed in the… 
Review
1995
Review
1995
De novo dup (5p) in a patient with congenital hypoplasia of the adrenal gland.
We report on a black male child with congenital hypoplasia of the adrenal gland (CHA) with a de novo duplication of 5p [dir dup(5… 
1994
1994
A rearrangement on chromosome 5 of an expressed human beta-glucuronidase pseudogene.
A novel transcript containing homology to exons 5, 9, 10, and 11 of the beta-glucuronidase gene has been shown to be derived from… 
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