- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1897-4287
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
PALB2: research reaching to clinical outcomes for women with breast cancer ; volume:14 ; number:1 ; day:19 ; month:4 ; year:2016 ; pages:1-7 ; date:12.2016
Hereditary cancer in clinical practice ; 14, Heft 1 (19.4.2016), 1-7, 12.2016
- Creator
-
Southey, Melissa C.
- Contributor
-
Winship, Ingrid
Nguyen-Dumont, Tú
SpringerLink (Online service)
- DOI
-
10.1186/s13053-016-0049-2
- URN
-
urn:nbn:de:1111-2016042125214
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:58 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
- Southey, Melissa C.
- Winship, Ingrid
- Nguyen-Dumont, Tú
- SpringerLink (Online service)
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Tumour morphology of early-onset breast cancers predicts breast cancer risk for first-degree relatives: the Australian Breast Cancer Family Registry
Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
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The PALB2 p.Leu939Trp mutation is not associated with breast cancer risk
The AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women
The utility of DNA extracted from saliva for genome-wide molecular research platforms
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Mammographic density and risk of breast cancer by mode of detection and tumor size: a case-control study
Self-rated health, epigenetic ageing, and long-term mortality in older Australians
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Rare genetic variants: making the connection with breast cancer susceptibility
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
Tumour morphology of early-onset breast cancers predicts breast cancer risk for first-degree relatives: the Australian Breast Cancer Family Registry
Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
Comparing the frequency of common genetic variants and haplotypes between carriers and non-carriers of BRCA1 and BRCA2deleterious mutations in Australian women diagnosed with breast cancer before 40 years of age
The PALB2 p.Leu939Trp mutation is not associated with breast cancer risk
The AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women
The utility of DNA extracted from saliva for genome-wide molecular research platforms
Mammographic density and risk of breast cancer by tumor characteristics: a case-control study
Mammographic density and risk of breast cancer by mode of detection and tumor size: a case-control study
Self-rated health, epigenetic ageing, and long-term mortality in older Australians