- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1465-542X
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Rare variants in the ATMgene and risk of breast cancer ; volume:13 ; number:4 ; day:25 ; month:7 ; year:2011 ; pages:1-9 ; date:8.2011
Breast cancer research ; 13, Heft 4 (25.7.2011), 1-9, 8.2011
- Contributor
-
Goldgar, David E.
Healey, Sue
Dowty, James G.
Da Silva, Leonard
Chen, Xiaoqing
Spurdle, Amanda B.
Terry, Mary Beth
Daly, Mary J.
Buys, Saundra M.
Southey, Melissa C.
Andrulis, Irene
John, Esther M.
Khanna, Kum Kum
Hopper, John L.
Oefner, Peter J.
Lakhani, Sunil
Chenevix-Trench, Georgia
SpringerLink (Online service)
- DOI
-
10.1186/bcr2919
- URN
-
urn:nbn:de:1111-2016032412458
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:49 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
- Goldgar, David E.
- Healey, Sue
- Dowty, James G.
- Da Silva, Leonard
- Chen, Xiaoqing
- Spurdle, Amanda B.
- Terry, Mary Beth
- Daly, Mary J.
- Buys, Saundra M.
- Southey, Melissa C.
- Andrulis, Irene
- John, Esther M.
- Khanna, Kum Kum
- Hopper, John L.
- Oefner, Peter J.
- Lakhani, Sunil
- Chenevix-Trench, Georgia
- 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
Tumour morphology of early-onset breast cancers predicts breast cancer risk for first-degree relatives: the 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
Rare genetic variants: making the connection with breast cancer susceptibility
Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATM
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
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 AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women
Heritable DNA methylation marks associated with susceptibility to breast cancer
The 4q27 locus and prostate cancer risk
Association of variably methylated tumour DNA regions with overall survival for invasive lobular breast cancer
Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
Tumour morphology of early-onset breast cancers predicts breast cancer risk for first-degree relatives: the 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
Rare genetic variants: making the connection with breast cancer susceptibility
Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATM
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
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 AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women
Heritable DNA methylation marks associated with susceptibility to breast cancer
The 4q27 locus and prostate cancer risk
Association of variably methylated tumour DNA regions with overall survival for invasive lobular breast cancer
Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
Tumour morphology of early-onset breast cancers predicts breast cancer risk for first-degree relatives: the 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
Rare genetic variants: making the connection with breast cancer susceptibility
Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATM
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
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 AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women
Heritable DNA methylation marks associated with susceptibility to breast cancer
The 4q27 locus and prostate cancer risk