On the development of a decision support intervention for mothers undergoing BRCA1/2 cancer genetic testing regarding communicating test results to their children

Author:

Peshkin Beth N.,DeMarco Tiffani A.,Tercyak Kenneth P.

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Reference40 articles.

1. Myriad Genetics Inc (2008) Annual shareholder report 2008. http://files.shareholder.com/downloads/MYGN/515983598x0-x239318/1DDB4C05-419A-400A-A121-545D02F86E6A/2008_Myriad_Annual_Report.pdf . Cited 14 Jan 2009

2. Antoniou A, Pharoah PD, Narod S et al (2003) 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. Am J Hum Genet 72:1117–1130

3. National Comprehensive Cancer Network (2009) NCCN clinical practice guidelines in oncology. Genetic/familial high-risk assessment: breast and ovarian–v.1.2009. http://www.nccn.org/professionals/physician_gls/PDF/genetics_screening.pdf . Cited 26 Jun 2009

4. Hallowell N, Ardern-Jones A, Eeles R et al (2005) Men’s decision-making about predictive BRCA1/2 testing: the role of family. J Genet Couns 14:207–217

5. Patenaude AF, Dorval M, DiGianni LS, Schneider KA, Chittenden A, Garber JE (2006) Sharing BRCA1/2 test results with first-degree relatives: factors predicting who women tell. J Clin Oncol 24:700–706

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