Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,168,521 papers from all fields of science
Search
Sign In
Create Free Account
5p13.3
A chromosome band present on 5p
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
5 relations
Chromosome 5 Short Arm
Chromosomes
GOLPH3 wt Allele
RNASEN wt Allele
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
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
C. Justice
,
Kevin Bishop
,
+6 authors
Alexander F. Wilson
G3: Genes, Genomes, Genetics
2016
Corpus ID: 8934992
Because of genetic heterogeneity present in idiopathic scoliosis, we previously defined clinical subsets (a priori) from a sample…
Expand
2014
2014
Structural Genomic Variation as Risk Factor for Idiopathic Recurrent Miscarriage
L. Nagirnaja
,
P. Palta
,
+7 authors
M. Laan
Human Mutation
2014
Corpus ID: 9940605
Recurrent miscarriage (RM) is a multifactorial disorder with acknowledged genetic heritability that affects ∼3% of couples aiming…
Expand
2014
2014
Novel genetic aberrations in breast phyllodes tumours: comparison between prognostically distinct groups
W. Tan
,
J. Lai
,
+7 authors
P. Tan
Breast Cancer Research and Treatment
2014
Corpus ID: 37593372
Phyllodes tumours of the breast are uncommon fibroepithelial neoplasms which pose management challenges due to difficulties in…
Expand
2011
2011
Gene Discovery in Nonsyndromic Cleft Lip with or without Cleft Palate
Brett T Chiquet
2011
Corpus ID: 82321487
2011
2011
Transmitted deletions of medial 5p and learning difficulties; Does the cadherin cluster only become penetrant when flanking genes are deleted?
J. Barber
,
Shuwen Huang
,
M. Bateman
,
A. Collins
American Journal of Medical Genetics. Part A
2011
Corpus ID: 25648367
The central portion of the short arm of chromosome 5 is unusual in that large, cytogenetically visible interstitial deletions…
Expand
2008
2008
A REANALYSIS OF 409 EUROPEAN-ANCESTRY AND AFRICAN AMERICAN SCHIZOPHRENIA PEDIGREES REVEALS SIGNIFICANT LINKAGE TO 8p23.3 WITH EVIDENCE OF LOCUS HETEROGENEITY
Elizabeth Holliday
,
B. Mowry
,
D. Nyholt
Schizophrenia Research
2008
Corpus ID: 6339003
The detection and replication of schizophrenia risk loci can require substantial sample sizes, which has prompted various…
Expand
2007
2007
Gain and overexpression of the oncostatin M receptor occur frequently in cervical squamous cell carcinoma and are associated with adverse clinical outcome
G. Ng
,
D. Winder
,
+6 authors
N. Coleman
Journal of Pathology
2007
Corpus ID: 21134882
For many oncogenes, increased expression resulting from copy number gain confers a selective advantage to cells that consequently…
Expand
Review
1995
Review
1995
De novo dup (5p) in a patient with congenital hypoplasia of the adrenal gland.
H. Chen
,
W. Hoffman
,
C. Kusyk
,
C. Tuck-Muller
,
M. Hoffman
,
L. Davis
American journal of medical genetics
1995
Corpus ID: 34269573
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…
Expand
1994
1994
A rearrangement on chromosome 5 of an expressed human beta-glucuronidase pseudogene.
C. Sargent
,
I. Chalmers
,
M. Leversha
,
N. Affara
Mammalian Genome
1994
Corpus ID: 13538920
A novel transcript containing homology to exons 5, 9, 10, and 11 of the beta-glucuronidase gene has been shown to be derived from…
Expand
1994
1994
A rearrangement on Chromosome 5 of an expressed human β-glucuronidase pseudogene
Carole A. Sargent
,
I. Chalmers
,
Margaret A. Leversha
,
N. Affara
Mammalian Genome
1994
Corpus ID: 21613776
A novel transcript containing homology to exons 5, 9, 10, and 11 of the β-glucuronidase gene has been shown to be derived from…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE