BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance, and the possibility of families whose cancer is not attributable to BRCA1 or BRCA2.

BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance, and the possibility of families whose cancer is not attributable to BRCA1 or BRCA2.

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http://www.wikidata.org/entity/Q35238541

Q35238541

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Molecular analysis of the BRCA1 and BRCA2 genes in 32 breast and/or ovarian cancer Spanish families Novel mutations in the BRCA1 and BRCA2 genes in Iranian women with early-onset breast cancer Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium A population study of mutations and LOH at breast cancer gene loci in tumours from sister pairs: two recurrent mutations seem to account for all BRCA1/BRCA2 linked breast cancer in Iceland.Recent advances in the understanding of the pathogenesis of serous carcinoma: the concept of low- and high-grade disease and the role of the fallopian tube.The application of nonsense-mediated mRNA decay inhibition to the identification of breast cancer susceptibility genes Clinical outcome of prophylactic oophorectomy in BRCA1/BRCA2 mutation carriers and events during follow-up.Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families.Hereditary ovarian carcinoma: heterogeneity, molecular genetics, pathology, and management.Loss of the BRCA1-interacting helicase BRIP1 results in abnormal mammary acinar morphogenesis.Triple-negative breast cancers: an updated review on treatment options Screening women at increased risk with MRI The fallopian tube: from back stage to center stage.Role of BRCA1 and BRCA2 mutations in pancreatic cancer.Recognizing BRCA gene mutation risk subsequent to breast cancer diagnosis in southwestern Ontario BRCA1 mutations in southern England Genetic tests to identify risk for breast cancer.Identification of novel BRCA founder mutations in Middle Eastern breast cancer patients using capture and Sanger sequencing analysis.Surrogate genetics and metabolic profiling for characterization of human disease alleles.Population genetics of BRCA1 and BRCA2.Germline Variants and Risk for Pancreatic Cancer: A Systematic Review and Emerging Concepts

P2860

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P2860

BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance, and the possibility of families whose cancer is not attributable to BRCA1 or BRCA2.

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http://www.wikidata.org/entity/Q35238541

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1997 nî lūn-bûn

@nan

1997 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

1997 թվականի մայիսին հրատարակված գիտական հոդված

@hy

1997年の論文

@ja

1997年論文

@yue

1997年論文

@zh-hant

1997年論文

@zh-hk

1997年論文

@zh-mo

1997年論文

@zh-tw

1997年论文

@wuu