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5p13.1

A chromosome band present on 5p
National Institutes of Health

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3 relations
Chromosome 5 Short ArmChromosomesPTGER4 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
An evaluation study of reported pancreatic adenocarcinoma risk-associated SNPs from genome-wide association studies in Chinese population.
2017
2017
Unusual de novo Partial Trisomy 17p12p11.2 due to Unbalanced Insertion into 5p13.1 in a Severely Affected Boy
Abstract Gain of copy numbers can be due to different chromosomal rearrangements such as direct or indirect duplications… 
2013
2013
Recapitulation of previous genome-wide association studies with two distinct pathophysiological entities of gastric cancer in the Korean population
Gastric cancer (GC) is the most common malignancy. The incidence rates remain remarkably high in East Asians. Although genome… 
2012
2012
40 Mb duplication in chromosome band 5p13.1p15.33 with 800 kb terminal deletion in a foetus with mild phenotypic features.
2012
2012
Further contributions towards the molecular analysis of NIPBL and SMC1A genes in a cohort of patients with Cornelia de Lange Syndrome
Dissertacao de Mestrado em Biologia apresentada a Faculdade de Ciencias da Universidade do Porto, 2012 
2011
2011
Implications of prenatal diagnosis of the fetus with both interstitial deletion and a small marker ring originating from chromosome 5
We describe a patient with 47,XY,del(5)(p11p13), +mar observed in prenatal screening. We performed analyses including G‐banding… 
2008
2008
M2041 The First Two Crohn's Disease Susceptibility Loci with a High Degree of Epistasis: PTGER4-Expression-Modulating Polymorphisms in the 5p13.1 Region Enhance ATG16L1-Associated Susceptibility to…
2007
2007
Fortuitous detection of a submicroscopic deletion at 1q25 in a girl with Cornelia‐de Lange syndrome carrying t(5;13)(p13.1;q12.1) by array‐based comparative genomic hybridization
We report on a 2‐year‐old Japanese girl with Cornelia‐de Lange syndrome (CdLS) who had mental and growth retardation, together… 
Review
2004
Review
2004
Unbalanced segregation of a complex four-break 5q23–31 insertion in the 5p13 band in a malformed child
A rec(5)dup(5)(q23.2q31.3) inherited from a maternal ins(5)(p13.1q23.2q31.3) was detected in a 4-month-old male child who showed… 
1995
1995
Chromosomal localization of the human prostanoid receptor gene family.
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