Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease ; volume:12 ; number:1 ; day:18 ; month:8 ; year:2011 ; pages:1-6 ; date:12.2011
BMC medical genetics ; 12, Heft 1 (18.8.2011), 1-6, 12.2011
- Creator
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Brønstad, Ingeborg
- Contributor
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Wolff, Anette SB
Løvås, Kristian
Knappskog, Per M.
Husebye, Eystein S.
SpringerLink (Online service)
- DOI
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10.1186/1471-2350-12-111
- URN
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urn:nbn:de:1111-2016071513336
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:45 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Brønstad, Ingeborg
- Wolff, Anette SB
- Løvås, Kristian
- Knappskog, Per M.
- Husebye, Eystein S.
- SpringerLink (Online service)
Other Objects (12)
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Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans
Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison’s disease in Sweden
Genome-wide algorithm for detecting CNV associations with diseases
A novel scatterplot-based method to detect copy number variation (CNV)
ClassifyCNV: a tool for clinical annotation of copy-number variants
dbCNV: deleteriousness-based model to predict pathogenicity of copy number variations
CTLA-4 as a genetic determinant in autoimmune Addison's disease
Analysis of cellular and humoral immune responses against cytomegalovirus in patients with autoimmune Addison’s disease
Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits
CNV Radar: an improved method for somatic copy number alteration characterization in oncology
MSeq-CNV: accurate detection of Copy Number Variation from Sequencing of Multiple samples
X-CNV: genome-wide prediction of the pathogenicity of copy number variations
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans
Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison’s disease in Sweden
Genome-wide algorithm for detecting CNV associations with diseases
A novel scatterplot-based method to detect copy number variation (CNV)
ClassifyCNV: a tool for clinical annotation of copy-number variants
dbCNV: deleteriousness-based model to predict pathogenicity of copy number variations
CTLA-4 as a genetic determinant in autoimmune Addison's disease
Analysis of cellular and humoral immune responses against cytomegalovirus in patients with autoimmune Addison’s disease
Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits
CNV Radar: an improved method for somatic copy number alteration characterization in oncology
MSeq-CNV: accurate detection of Copy Number Variation from Sequencing of Multiple samples
X-CNV: genome-wide prediction of the pathogenicity of copy number variations
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans
Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison’s disease in Sweden
Genome-wide algorithm for detecting CNV associations with diseases
A novel scatterplot-based method to detect copy number variation (CNV)
ClassifyCNV: a tool for clinical annotation of copy-number variants
dbCNV: deleteriousness-based model to predict pathogenicity of copy number variations
CTLA-4 as a genetic determinant in autoimmune Addison's disease
Analysis of cellular and humoral immune responses against cytomegalovirus in patients with autoimmune Addison’s disease
Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits
CNV Radar: an improved method for somatic copy number alteration characterization in oncology