- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1465-542X
- Extent
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Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Increased copy number at 3p14 in breast cancer ; volume:7 ; number:5 ; day:6 ; month:7 ; year:2005 ; pages:1-9 ; date:10.2005
Breast cancer research ; 7, Heft 5 (6.7.2005), 1-9, 10.2005
- Creator
-
Ljuslinder, Ingrid
- Contributor
-
Malmer, Beatrice
Golovleva, Irina
Thomasson, Marcus
Grankvist, Kjell
Höckenström, Thomas
Emdin, Stefan
Jonsson, Yvonne
Hedman, Håkan
Henriksson, Roger
SpringerLink (Online service)
- DOI
-
10.1186/bcr1279
- URN
-
urn:nbn:de:1111-2016032356975
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:50 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Ljuslinder, Ingrid
- Malmer, Beatrice
- Golovleva, Irina
- Thomasson, Marcus
- Grankvist, Kjell
- Höckenström, Thomas
- Emdin, Stefan
- Jonsson, Yvonne
- Hedman, Håkan
- Henriksson, Roger
- SpringerLink (Online service)
Other Objects (12)
Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
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Mitochondrial DNA copy number instability in ERBB2-amplified breast cancer tumors
Expanding the genetic basis of copy number variation in familial breast cancer
Germline DNA copy number variation in familial and early-onset breast cancer
Somatic mutation and gain of copy number of PIK3CA in human breast cancer
Genomic copy number alterations as biomarkers for triple negative pregnancy-associated breast cancer
Breast tumor copy number aberration phenotypes and genomic instability
High leukocyte mitochondrial DNA copy number contributes to poor prognosis in breast cancer patients
Landscape of somatic allelic imbalances and copy number alterations in HER2-amplified breast cancer
Histotype-specific copy-number alterations in ovarian cancer
Germline copy number variants and endometrial cancer risk
Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
Comprehensive copy number profiles of breast cancer cell model genomes
Mitochondrial DNA copy number instability in ERBB2-amplified breast cancer tumors
Expanding the genetic basis of copy number variation in familial breast cancer
Germline DNA copy number variation in familial and early-onset breast cancer
Somatic mutation and gain of copy number of PIK3CA in human breast cancer
Genomic copy number alterations as biomarkers for triple negative pregnancy-associated breast cancer
Breast tumor copy number aberration phenotypes and genomic instability
High leukocyte mitochondrial DNA copy number contributes to poor prognosis in breast cancer patients
Landscape of somatic allelic imbalances and copy number alterations in HER2-amplified breast cancer
Histotype-specific copy-number alterations in ovarian cancer
Germline copy number variants and endometrial cancer risk
Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
Comprehensive copy number profiles of breast cancer cell model genomes
Mitochondrial DNA copy number instability in ERBB2-amplified breast cancer tumors
Expanding the genetic basis of copy number variation in familial breast cancer
Germline DNA copy number variation in familial and early-onset breast cancer
Somatic mutation and gain of copy number of PIK3CA in human breast cancer
Genomic copy number alterations as biomarkers for triple negative pregnancy-associated breast cancer
Breast tumor copy number aberration phenotypes and genomic instability
High leukocyte mitochondrial DNA copy number contributes to poor prognosis in breast cancer patients
Landscape of somatic allelic imbalances and copy number alterations in HER2-amplified breast cancer
Histotype-specific copy-number alterations in ovarian cancer