Familial Breast Cancer
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- 2010
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Mark
Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.
- Contribution to journal › Article
- 2008
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Mark
Recurrent gross mutations of the PTEN tumor suppressor gene in breast cancers with deficient DSB repair
- Contribution to journal › Article
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Mark
Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH).
- Contribution to journal › Article
- 2007
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Mark
Tumor genome wide DNA alterations assessed by array CGH in patients with poor and excellent survival following operation for colorectal cancer
- Contribution to journal › Article
- 2004
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Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
- Contribution to journal › Article
- 2001
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Mark
Gene-expression profiles in hereditary breast cancer
- Contribution to journal › Article
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Mark
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
- Contribution to journal › Article
- 2000
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Mark
A hypersensitive estrogen receptor-alpha mutation in premalignant breast lesions
- Contribution to journal › Article
- 1998
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Mark
Steroid receptors in hereditary breast carcinomas associated with BRCA1 or BRCA2 mutations or unknown susceptibility genes
- Contribution to journal › Article
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Mark
BRCA2 germ-line mutations are frequent in male breast cancer patients without a family history of the disease
- Contribution to journal › Article
