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16q23.1
A chromosome band present on 16q
National Institutes of Health
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Related topics
Related topics
4 relations
16q
CTRB1 wt Allele
Chromosomes
TERF2IP wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Cross-Cancer Pleiotropic Analysis Reveals Novel Susceptibility Loci for Lung Cancer
Lijuan Wang
,
Meng Zhu
,
+10 authors
Hongbing Shen
Frontiers in Oncology
2020
Corpus ID: 210173008
Genome-wide association studies (GWASs) have identified hundreds of single nucleotide polymorphisms (SNPs) associated with cancer…
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2017
2017
Генетические маркеры метаболического синдрома и коронарного атеросклероза у жителей Якутии
А. Н. Романова
,
Михаил Иванович Воевода
,
В. Н. Максимов
2017
Corpus ID: 79922468
Aim. Evaluation of the association of rs17465637 gene MIA3 (1q41), rs4804611 gene ZNF627 (19p13.2), rs2549513 (16q23.1…
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2013
2013
The first report of nephrocalcinosis in a patient with a 16q23.1-16q23.3 deletion, global developmental delay, trigonocephaly, and portocaval shunt.
R. Jobling
,
P. Kannu
,
C. Licht
,
M. Carter
Clinical Dysmorphology
2013
Corpus ID: 30589619
Clinical summary Our patient is a 4-year-old boy born to a healthy 27-yearold G4P3L3 mother. The pregnancy was complicated by…
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2012
2012
Comprehensive cytogenetic study of primary cutaneous gamma-delta T-cell lymphoma by means of spectral karyotyping and genome-wide single nucleotide polymorphism array.
Mio Yamamoto‐Sugitani
,
J. Kuroda
,
+11 authors
M. Taniwaki
Cancer Genetics
2012
Corpus ID: 29696012
2010
2010
A polymorphism rs17336700 in the PSMD7 gene is associated with ankylosing spondylitis in Chinese subjects
Z. Niu
,
R. Lei
,
+6 authors
Wei Huang
Annals of the Rheumatic Diseases
2010
Corpus ID: 27432119
Ankylosing spondylitis (AS) is an inflammatory rheumatic disease and strongly associated with human leucocyte antigen (HLA)-B27.1…
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2010
2010
ome-Wide Catalogue of Chromosomal Aberrations in rett's Esophagus and Esophageal Adenocarcinoma: igh-Density Single Nucleotide Polymorphism
J. Ajani
,
E. Hawk
,
+6 authors
Xifeng Wu
2010
Corpus ID: 22089742
nloaded better understand the molecular mechanisms behind esophageal adenocarcinoma (EAC) tumoris, we used high-density single…
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2007
2007
Dissecting the heterogeneity of rheumatoid arthritis through linkage analysis of quantitative traits.
L. Criswell
,
W. Chen
,
+5 authors
C. Amos
Arthritis & Rheumatism
2007
Corpus ID: 35333792
OBJECTIVE To dissect the heterogeneity of rheumatoid arthritis (RA) through linkage analysis of quantitative traits, specifically…
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2007
2007
Genome Wide-DNA Profiling of HIV-Related Non-Hodgkin Lymphomas: Implications for Disease Pathogenesis and Histogenesis.
F. Bertoni
,
G. Poretti
,
+9 authors
G. Gaidano
2007
Corpus ID: 208461923
Non-Hodgkin’s lymphomas (NHL) represent a frequent complication of HIV infection and a major source of morbidity and mortality…
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2004
2004
Autosomal lesions versus fragile sites
P. Howard‐Peebles
Human Genetics
2004
Corpus ID: 7542834
Wegner (1983) and Rudduck and Franz6n (1983) recently reported "a new heritable fragile site on human chromosome 3." Both reports…
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Review
2001
Review
2001
Human hepatocellular carcinoma is characterized by a highly consistent pattern of genomic imbalances, including frequent loss of 16q23.1–24.1
B. Balsara
,
J. Pei
,
+9 authors
J. Testa
Genes, Chromosomes and Cancer
2001
Corpus ID: 22167647
Comparative genomic hybridization (CGH) analysis was used to identify chromosomal imbalances in 52 human primary hepatocellular…
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