Etiology of familial breast cancer with undetected BRCA1 and BRCA2 mutations: clinical implications.
about
Prevalence of Germline Mutations in Genes Engaged in DNA Damage Repair by Homologous Recombination in Patients with Triple-Negative and Hereditary Non-Triple-Negative Breast CancersGenomic rearrangement screening of the BRCA1 from seventy Iranian high-risk breast cancer families.A novel loss-of-function heterozygous BRCA2 c.8946_8947delAG mutation found in a Chinese woman with family history of breast cancer.BRCA1/2-negative hereditary triple-negative breast cancers exhibit BRCAness.The cancer genome: from structure to function.Identification of miR-10b, miR-26a, miR-146a and miR-153 as potential triple-negative breast cancer biomarkers.Decreased CDK10 expression correlates with lymph node metastasis and predicts poor outcome in breast cancer patients - a short report.BRCA1 c.68_69delAG (exon2), c.181T>G (exon5), c.798_799delTT and 943ins10 (exon11) mutations in Burkina Faso
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P2860
Etiology of familial breast cancer with undetected BRCA1 and BRCA2 mutations: clinical implications.
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2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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name
Etiology of familial breast ca ...... ations: clinical implications.
@en
Etiology of familial breast ca ...... ations: clinical implications.
@nl
type
label
Etiology of familial breast ca ...... ations: clinical implications.
@en
Etiology of familial breast ca ...... ations: clinical implications.
@nl
prefLabel
Etiology of familial breast ca ...... ations: clinical implications.
@en
Etiology of familial breast ca ...... ations: clinical implications.
@nl
P2860
P1433
P1476
Etiology of familial breast ca ...... ations: clinical implications.
@en
P2093
Eugenia Yiannakopoulou
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P2888
P356
10.1007/S13402-013-0158-0
P577
2013-12-04T00:00:00Z