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20q13.33
A chromosome band present on 20q
National Institutes of Health
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Related topics
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7 relations
20q
Chromosomes
GATA5 wt Allele
MIR1-1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Microarray CGH analysis of hematological patients with del(20q)
Chun-xiao Wu
,
Jinlan Pan
,
+8 authors
Y. Gong
International journal of hematology
2015
Corpus ID: 7616326
Deletion of the long arm of chromosome 20 is a common abnormality underlying hematological malignancy. We analyzed 21 patients…
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Review
2013
Review
2013
Qualitative and quantitative expression status of the human chromosome 20 genes in cancer tissues and the representative cell lines.
Quanhui Wang
,
Bo Wen
,
+40 authors
Siqi Liu
Journal of Proteome Research
2013
Corpus ID: 26411469
Under the guidance of the Chromosome-centric Human Proteome Project (C-HPP), (1, 2) we conducted a systematic survey of the…
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2013
2013
Additional evidence to support the role of the 20q13.33 region in susceptibility to autism
Anne-Laure Mosca-Boidron
,
M. Valduga
,
+13 authors
L. Faivre
American Journal of Medical Genetics. Part A
2013
Corpus ID: 34806584
Additional Evidence to Support the Role of the 20q13.33 Region in Susceptibility to Autism Anne-Laure Mosca-Boidron,* Myl ene…
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2012
2012
Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients.
S. Lubbe
,
N. Whiffin
,
I. Chandler
,
P. Broderick
,
R. Houlston
Carcinogenesis
2012
Corpus ID: 17694472
Recent genome-wide association studies have identified single-nucleotide polymorphisms at 16 genetic loci associated with…
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2012
2012
PSMA7 inhibits the tumorigenicity of A549 human lung adenocarcinoma cells
Jia-yu Tan
,
Xiang Huang
,
Ya-ling Luo
Molecular and Cellular Biochemistry
2012
Corpus ID: 15172470
The gene for proteasome subunit alpha type-7 (PSMA7) is located in chromosomal 20q13.33, a region frequently amplified in tumor…
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2012
2012
Association Analysis of Single Nucleotide Polymorphisms at Five Loci: Comparison between Atopic Dermatitis and Asthma in the Chinese Han Population
Huayang Tang
,
Xianfa Tang
,
+10 authors
Xuejun Zhang
PLoS ONE
2012
Corpus ID: 1622636
Atopic diseases, such as atopic dermatitis (AD) and asthma, are closely related to clinical phenotypes with hypersensitivity, and…
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2012
2012
Genetic variant rs4982958 at 14q11.2 is associated with allergic rhinitis in a Chinese Han population running title: 14q11.2 is a susceptibility locus for allergic rhinitis.
Xianfa Tang
,
Tang Hy
,
+12 authors
Zhang Xj
Journal of investigational allergology & clinical…
2012
Corpus ID: 12906878
BACKGROUND Allergic rhinitis (AR) is one of the most common diseases caused by the combined effects of intrinsic factors…
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2011
2011
De Novo Deletion of Chromosome 20q13.33 in a Patient with Tracheo-esophageal Fistula, Cardiac Defects and Genitourinary Anomalies Implicates GTPBP5 as a Candidate Gene
B. Solomon
,
D. Pineda-Alvarez
,
+6 authors
S. Chandrasekharappa
Birth defects research. Clinical and molecular…
2011
Corpus ID: 16538936
BACKGROUND Tracheo-esophageal fistula (TEF) with/or without esophageal atresia (EA) is a common congenital malformation that is…
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Highly Cited
2010
Highly Cited
2010
Interaction between 5 genetic variants and allergy in glioma risk.
M. Schoemaker
,
Lindsay B. Robertson
,
+13 authors
A. Swerdlow
American Journal of Epidemiology
2010
Corpus ID: 39172729
The etiology of glioma is barely known. Epidemiologic studies have provided evidence for an inverse relation between glioma risk…
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Review
2007
Review
2007
A de novo 1.1–1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features
F. Béna
,
A. Bottani
,
Fabienne Marcelli
,
Loredana D'Amato Sizonenko
,
B. Conrad
,
S. Dahoun
American Journal of Medical Genetics. Part A
2007
Corpus ID: 38939655
We report on a de novo submicroscopic deletion of 20q13.33 identified by subtelomeric fluorescence in situ hybridization (FISH…
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