BRCAl Screening in Patients with a Family History of Breast or Ovarian Cancer
Author:
Publisher
Mary Ann Liebert Inc
Subject
Genetics(clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/gte.1999.3.223
Reference19 articles.
1. Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer
2. BRCA2 germline mutations in Swedish breast cancer families
3. Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families
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1. Prevalence of BRCA1 and BRCA2 pathogenic variants in a large, unselected breast cancer cohort;International Journal of Cancer;2018-11-09
2. Parent of Origin and Prognosis in Familial Breast Cancer in Sweden;ANTICANCER RES;2017
3. A hypothesis-generating search for new genetic breast cancer syndromes a national study in 803 Swedish families;Hereditary Cancer in Clinical Practice;2007
4. Family History, and Impact on Clinical Presentation and Prognosis, in a Population-based Breast Cancer Cohort from the Stockholm County;Familial Cancer;2006-07-01
5. High incidence of skewed X chromosome inactivation in young patients with familial non-BRCA1/BRCA2 breast cancer;Journal of Medical Genetics;2005-06-15
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