BRCA1 mutations and other sequence variants in a population-based sample of Australian women with breast cancer
about
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studiesAfter BRCA1 and BRCA2-what next? Multifactorial segregation analyses of three-generation, population-based Australian families affected by female breast cancer.Log odds of carrying an Ancestral Mutation in BRCA1 or BRCA2 for a Defined personal and family history in an Ashkenazi Jewish woman (LAMBDA)Prevalence of BRCA1 in a hospital-based population of Dutch breast cancer patientsNovel sequence variants and a high frequency of recurrent polymorphisms in BRCA1 gene in Sri Lankan breast cancer patients and at risk individuals.Constitutional methylation of the BRCA1 promoter is specifically associated with BRCA1 mutation-associated pathology in early-onset breast cancer.Prevalence of BRCA1 and BRCA2 mutations in Korean breast cancer patients.FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancer.A PALB2 mutation associated with high risk of breast cancer.Morphological predictors of BRCA1 germline mutations in young women with breast cancer.Tobacco use and cancer: an epidemiologic perspective for geneticists.Contribution of large genomic BRCA1 alterations to early-onset breast cancer selected for family history and tumour morphology: a report from The Breast Cancer Family Registry.Population-based estimate of the contribution of TP53 mutations to subgroups of early-onset breast cancer: Australian Breast Cancer Family Study.Methylation of Breast Cancer Predisposition Genes in Early-Onset Breast Cancer: Australian Breast Cancer Family Registry.BRCA1 promoter deletions in young women with breast cancer and a strong family history: a population-based studyBRCA1 and BRCA2 mutations in Turkish breast/ovarian families and young breast cancer patients.Mutations of the BRCA1 and BRCA2 genes in patients with bilateral breast cancer.Tumour morphology predicts PALB2 germline mutation status.Genetic 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.BRCA1 and BRCA2 mutation carriers in the Breast Cancer Family Registry: an open resource for collaborative researchIncreased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry.Comparison of DNA- and RNA-based methods for detection of truncating BRCA1 mutations.A comprehensive focus on global spectrum of BRCA1 and BRCA2 mutations in breast cancer.BRCA1 and BRCA2 germline mutations in 85 Iranian breast cancer patients.Allelic imbalance in BRCA1 and BRCA2 gene expression is associated with an increased breast cancer risk.Familial Risks, Early-Onset Breast Cancer, and BRCA1 and BRCA2 Germline MutationsDiscordant pattern ofBRCA1gene epimutation in blood between mothers and daughters
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P2860
BRCA1 mutations and other sequence variants in a population-based sample of Australian women with breast cancer
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
BRCA1 mutations and other sequ ...... alian women with breast cancer
@ast
BRCA1 mutations and other sequ ...... alian women with breast cancer
@en
type
label
BRCA1 mutations and other sequ ...... alian women with breast cancer
@ast
BRCA1 mutations and other sequ ...... alian women with breast cancer
@en
prefLabel
BRCA1 mutations and other sequ ...... alian women with breast cancer
@ast
BRCA1 mutations and other sequ ...... alian women with breast cancer
@en
P2093
P2860
P50
P356
P1476
BRCA1 mutations and other sequ ...... alian women with breast cancer
@en
P2093
Andersen CR
Jennings KM
Maskiell JA
McCredie MR
Tesoriero AA
P2860
P2888
P356
10.1038/SJ.BJC.6690008
P407
P577
1999-01-01T00:00:00Z