Variants of unknown significance in BRCA testing: impact on risk perception, worry, prevention and counseling
Author:
Publisher
Elsevier BV
Subject
Oncology,Hematology
Link
http://academic.oup.com/annonc/article-pdf/24/suppl_8/viii69/6676486/mdt312.pdf
Reference18 articles.
1. 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 studies;Antoniou;Am J Hum Genet,2003
2. Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results;Plon;Hum Mutat,2008
3. Genetic variants of uncertain significance: flies in the ointment;Domchek;J Clin Oncol,2008
4. Breast cancer gene variants: separating the harmful from the harmless;Domchek;J Clin Invest,2009
5. Unclassified variants in BRCA genes: guidelines for interpretation;Radice;Ann Oncol,2011
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