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2q36.3
A chromosome band present on 2q
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosomes
DNER wt Allele
TRIP12 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family.
K. Ramzan
,
F. Imtiaz
,
+4 authors
M. Al‐Owain
International Journal of Pediatric…
2014
Corpus ID: 21137956
Review
2013
Review
2013
A novel COL4A3 mutation causes autosomal-recessive Alport syndrome in a large Turkish family.
A. Uzak
,
B. Tokgoz
,
M. Dundar
,
M. Tekin
Genetic Testing and Molecular Biomarkers
2013
Corpus ID: 11433920
BACKGROUND Alport syndrome (AS) is a genetically heterogeneous disorder that is characterized by hematuria, progressive renal…
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2012
2012
Common Variants in the COL4A4 Gene Confer Susceptibility to Lattice Degeneration of the Retina
A. Meguro
,
H. Ideta
,
+14 authors
N. Mizuki
PLoS ONE
2012
Corpus ID: 2883064
Lattice degeneration of the retina is a vitreoretinal disorder characterized by a visible fundus lesion predisposing the patient…
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2011
2011
Variantes genéticas, riesgo cardiovascular y estudios de asociación de genoma completo
O. Companioni
,
F. R. Esparragón
,
A. M. Fernández-Aceituno
,
J. Pérez
2011
Corpus ID: 115790687
2009
2009
Association of three polymorphisms selected from a genome-wide association study with coronary heart disease in the Tunisian population
Lakhdar Ghazouani
,
S. Khalifa
,
+6 authors
T. Mahjoub
Journal of Thrombosis and Thrombolysis
2009
Corpus ID: 2960451
Despite extensive exploration of many genes, strong evidence of a molecular genetic association with coronary heart disease (CHD…
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2009
2009
Abstract 1882: Chromosome 6q25.1 and 2q36.3 Coronary Heart Disease Risk Loci Are Associated With Altered Cardiac Gene Expression Profiles in Normal Heart
A. Pilbrow
,
J. Pearson
,
+8 authors
V. Cameron
2009
Corpus ID: 84011698
Genome-wide association studies have identified three chromosomal loci, 9p21.3, 6q25.1 and 2q36.3, that are strongly associated…
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2009
2009
Clinical and Population Studies Large Scale Association Analysis of Novel Genetic Loci for Coronary Artery Disease Coronary Artery Disease Consortium *
2009
Corpus ID: 3879484
Background—Combined analysis of 2 genome-wide association studies in cases enriched for family history recently identified 7 loci…
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2008
2008
Deletion 2q36.2q36.3 with multiple renal cysts and severe mental retardation.
M. Doco‐Fenzy
,
E. Landais
,
+14 authors
D. Gaillard
European Journal of Medical Genetics
2008
Corpus ID: 24033193
2007
2007
Maladies héréditaires du métabolisme vitaminosensibles chez l'adulte. Implications diagnostiques et thérapeutiques
V. Valayannopoulos
,
S. Romano
,
+6 authors
P. Lonlay
2007
Corpus ID: 72286554
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