Genetic testing in the context of the revision of the French law on bioethics

Pathologie-biologie
D BonneauD Stoppa-Lyonnet

Abstract

This article focuses on six questions raised by genetic testing in human: (1) the use of genetic tests, (2) information given to relatives of patients affected with genetic disorders, (3) prenatal and preimplantatory diagnosis for late onset genetic diseases and the use of pangenomic tests in prenatal diagnosis, (4) direct-to-consumer genetic testing, (5) population screening in the age of genomic medicine and (6) incidental findings when genetic testing are used.

References

Jan 3, 2003·The New England Journal of Medicine·Muin J KhouryEdward R B McCabe
Oct 16, 2004·Annual Review of Genomics and Human Genetics·Linda L McCabe, Edward R B McCabe
Jan 12, 2008·Annual Review of Medicine·Linda L McCabe, Edward R B McCabe
Apr 29, 2008·Bulletin of the World Health Organization·Anne AndermannVéronique Déry

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Citations

Aug 9, 2011·Cambridge Quarterly of Healthcare Ethics : CQ : the International Journal of Healthcare Ethics Committees·Bette Anton
Jan 26, 2012·European Journal of Human Genetics : EJHG·Pascal BorryHeidi Howard
Jan 17, 2016·Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie·C Coubes

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