Cancer incidence in relatives of a population-based set of cases of early-onset breast cancer with a known BRCA1 and BRCA2 mutation status
about
Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear familyAssociations of high-grade prostate cancer with BRCA1 and BRCA2 founder mutationsContribution of the Defective BRCA1, BRCA2 and CHEK2 Genes to the Familial Aggregation of Breast Cancer: a Simulation Study Based on the Swedish Family-Cancer DatabasePresymptomatic breast cancer in Egypt: role of BRCA1 and BRCA2 tumor suppressor genes mutations detection.Breast cancer patients with lobular cancer more commonly have a father than a mother diagnosed with cancer.Founder and Recurrent Mutations in BRCA1 and BRCA2 Genes in Latin American Countries: State of the Art and Literature Review.Family history of breast cancer in relation to tumor characteristics and mortality in a population-based study of young women with invasive breast cancerDo Breast Cancer Patients Tested in the Oncology Care Setting Share BRCA Mutation Results with Family Members and Health Care Providers?Genetic testing and first presymptomatic diagnosis in Moroccan families at high risk for breast/ovarian cancer.Rare germline mutations in the BRCA2 gene are associated with early-onset prostate cancer.Tumour morphology of early-onset breast cancers predicts breast cancer risk for first-degree relatives: the Australian Breast Cancer Family Registry.The role of the BRCA2 gene in susceptibility to prostate cancer revisitedGenetic counselling and testing for inherited gene mutations in newly diagnosed patients with breast cancer: a review of the existing literature and a proposed research agenda.Skin cancer risk in BRCA1/2 mutation carriers.The association between prognosis of breast cancer and first-degree family history of breast or ovarian cancer: a systematic review and meta-analysis.Novel germline BRCA1 and BRCA2 mutations in Turkish women with breast and/or ovarian cancer and their relatives.Estimate of the penetrance of BRCA mutation and the COS software for the assessment of BRCA mutation probability.Etiology of familial breast cancer with undetected BRCA1 and BRCA2 mutations: clinical implications.Familial and sporadic breast cancers: differences in clinical, histopathological, and immunohistochemical features.
P2860
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P2860
Cancer incidence in relatives of a population-based set of cases of early-onset breast cancer with a known BRCA1 and BRCA2 mutation status
description
2003 nî lūn-bûn
@nan
2003 թուականին հրատարակուած գիտական յօդուած
@hyw
2003 թվականին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Cancer incidence in relatives ...... RCA1 and BRCA2 mutation status
@ast
Cancer incidence in relatives ...... RCA1 and BRCA2 mutation status
@en
Cancer incidence in relatives ...... RCA1 and BRCA2 mutation status
@nl
type
label
Cancer incidence in relatives ...... RCA1 and BRCA2 mutation status
@ast
Cancer incidence in relatives ...... RCA1 and BRCA2 mutation status
@en
Cancer incidence in relatives ...... RCA1 and BRCA2 mutation status
@nl
prefLabel
Cancer incidence in relatives ...... RCA1 and BRCA2 mutation status
@ast
Cancer incidence in relatives ...... RCA1 and BRCA2 mutation status
@en
Cancer incidence in relatives ...... RCA1 and BRCA2 mutation status
@nl
P2093
P2860
P356
P1476
Cancer incidence in relatives ...... RCA1 and BRCA2 mutation status
@en
P2093
Anna Bladström
Niklas Loman
Oskar Johannsson
P2860
P2888
P304
P356
10.1186/BCR632
P407
P50
P577
2003-01-01T00:00:00Z
P5875
P6179
1022841183