Common genomic variants associated with breast cancer predict the risk of second primary breast cancer diagnosis
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1897-4287
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Common genomic variants associated with breast cancer predict the risk of second primary breast cancer diagnosis ; volume:10 ; number:2 ; day:12 ; month:4 ; year:2012 ; pages:1-2 ; date:12.2012
Hereditary cancer in clinical practice ; 10, Heft 2 (12.4.2012), 1-2, 12.2012
- Creator
-
Sawyer, S.
- Contributor
-
McKinley, J.
Mitchell, G.
Chenevix-Trench, G.
Harris, M.
Lindeman, G.
James, PA
SpringerLink (Online service)
- DOI
-
10.1186/1897-4287-10-S2-A28
- URN
-
urn:nbn:de:1111-2016073117593
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:00 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
- Sawyer, S.
- McKinley, J.
- Mitchell, G.
- Chenevix-Trench, G.
- Harris, M.
- Lindeman, G.
- James, PA
- SpringerLink (Online service)
Other Objects (12)
E-cadherin genetic variants predict survival outcome in breast cancer patients
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
GnRH and LHRgene variants predict adverse outcome in premenopausal breast cancer patients
Genetic variants associated with breast size also influence breast cancer risk
Breast cancer gene variants and the susceptibilkity to cervical cancer
Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception
Disulfidptosis-associated lncRNAs predict breast cancer subtypes
Genomic pathways modulated by Twist in breast cancer
Breast cancer
Breast cancer
Breast cancer
E-cadherin genetic variants predict survival outcome in breast cancer patients
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
GnRH and LHRgene variants predict adverse outcome in premenopausal breast cancer patients
Genetic variants associated with breast size also influence breast cancer risk
Breast cancer gene variants and the susceptibilkity to cervical cancer
Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception
Disulfidptosis-associated lncRNAs predict breast cancer subtypes
Genomic pathways modulated by Twist in breast cancer
Breast cancer
Breast cancer
Breast cancer
E-cadherin genetic variants predict survival outcome in breast cancer patients
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
GnRH and LHRgene variants predict adverse outcome in premenopausal breast cancer patients
Genetic variants associated with breast size also influence breast cancer risk
Breast cancer gene variants and the susceptibilkity to cervical cancer
Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception
Disulfidptosis-associated lncRNAs predict breast cancer subtypes
Genomic pathways modulated by Twist in breast cancer
Breast cancer
Breast cancer