The androgen receptor CAG repeat polymorphism and modification of breast cancer risk in BRCA1 and BRCA2 mutation carriers
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1465-542X
- Extent
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Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
The androgen receptor CAG repeat polymorphism and modification of breast cancer risk in BRCA1 and BRCA2 mutation carriers ; volume:7 ; number:2 ; day:16 ; month:12 ; year:2004 ; pages:1-8 ; date:4.2005
Breast cancer research ; 7, Heft 2 (16.12.2004), 1-8, 4.2005
- Contributor
-
Spurdle, Amanda B.
Antoniou, Antonis C.
Duffy, David L.
Pandeya, Nirmala
Kelemen, Livia
Chen, Xiaoqing
Peock, Susan
Cook, Margaret R.
Smith, Paula L.
Purdie, David M.
Newman, Beth
Dite, Gillian S.
Apicella, Carmel
Southey, Melissa C.
Giles, Graham G.
Hopper, John L.
Chenevix-Trench, Georgia
Easton, Douglas F.
SpringerLink (Online service)
- DOI
-
10.1186/bcr971
- URN
-
urn:nbn:de:1111-2016032355879
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:45 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
- Spurdle, Amanda B.
- Antoniou, Antonis C.
- Duffy, David L.
- Pandeya, Nirmala
- Kelemen, Livia
- Chen, Xiaoqing
- Peock, Susan
- Cook, Margaret R.
- Smith, Paula L.
- Purdie, David M.
- Newman, Beth
- Dite, Gillian S.
- Apicella, Carmel
- Southey, Melissa C.
- Giles, Graham G.
- Hopper, John L.
- Chenevix-Trench, Georgia
- Easton, Douglas F.
- SpringerLink (Online service)
Other Objects (12)
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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
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
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The AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women
Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATM
BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families
Heritable DNA methylation marks associated with susceptibility to breast cancer
Association of variably methylated tumour DNA regions with overall survival for invasive lobular breast cancer
PALB2: research reaching to clinical outcomes for women with breast cancer
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
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
The 4q27 locus and prostate cancer risk
The AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women
Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATM
BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families
Heritable DNA methylation marks associated with susceptibility to breast cancer
Association of variably methylated tumour DNA regions with overall survival for invasive lobular breast cancer
PALB2: research reaching to clinical outcomes for women with breast cancer
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
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
The 4q27 locus and prostate cancer risk
The AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women
Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATM
BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families
Heritable DNA methylation marks associated with susceptibility to breast cancer
Association of variably methylated tumour DNA regions with overall survival for invasive lobular breast cancer