Genetic diseases and information to relatives: practical and ethical issues for professionals after introduction of a legal framework in France
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/s41431-018-0103-9.pdf
Reference23 articles.
1. D’Audiffret Van Haecke D, de Montgolfier S. Genetic test results and disclosure to family members: qualitative interviews of healthcare professionals’ perceptions of ethical and professional issues in France. J Genet Couns. 2016;25:483–94. https://doi.org/10.1007/s10897-015-9896-7 .
2. Weil-Dubuc P-L, Les servitudes du droit de savoir, La Vie Des Idées, 2013. Retrieved from http://www.laviedesidees.fr/Les-servitudes-du-droit-de-savoir.html .
3. Gaff CL, Clarke AJ, Atkinson P, et al. Process and outcome in communication of genetic information within families: a systematic review. Eur J Human Genet. 2007;15:999–1011. https://doi.org/10.1038/sj.ejhg.5201883 .
4. Resta RG. Defining and redefining the scope and goals of genetic counseling. Am J Med Genet Part C, Semin Med Genet. 2006;142C:269–75. https://doi.org/10.1002/ajmg.c.30093 .
5. Forrest LE, Delatycki MB, Skene L, Aitken M. Communicating genetic information in families—a review of guidelines and position papers. Eur J Human Genet. 2007;15:612–8. https://doi.org/10.1038/sj.ejhg.5201822 .
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