N. H. Anderson, Fondation of integration theory, 1981.

R. T. Anderson, N. Press, D. C. Tucker, B. M. Snively, L. Wenzel et al., Patient acceptability of genotypic testing for hemochromatosis in primary care, Genetics In Medicine: Official Journal Of The American College Of Medical Genetics, vol.7, issue.8, pp.557-563, 2005.

M. Bruno, M. Digennaro, S. Tommasi, B. Stea, T. Danese et al., Attitude towards genetic testing for breast cancer susceptibility: a comparison of affected and unaffected women, European Journal of Cancer Care, vol.19, issue.3, pp.360-368, 2010.

F. M. Facio, H. Eidem, T. Fisher, S. Brooks, A. Linn et al., Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study, European Journal of Human Genetics, vol.21, issue.3, pp.261-265, 2013.
DOI : 10.1038/ejhg.2012.179
URL : https://www.nature.com/articles/ejhg2012179.pdf

, Règles de bonnes pratiques en génétique constitutionnelle à des fins médicales (Hors diagnostic prénatal), Consulté 9 juillet 2015, 2013.

S. K. Peterson, The role of the family in genetic testing: theoretical perspectives, current knowledge, and future directions. Health Education & Behavior: The Official Publication of the Society for Public Health Education, vol.32, pp.627-639, 2005.

S. J. Roberts, S. A. Larusse, H. Katzen, P. J. Whitehouse, M. Barber et al., Reasons for Seeking Genetic Susceptibility Testing Among First-Degree Relatives of People With Alzheimer Disease, Alzheimer Disease & Associated Disorders, vol.17, issue.2, pp.86-93, 2003.

J. S. Shaw and K. L. Bassi, Lay Attitudes toward Genetic Testing for Susceptibility to Inherited Diseases, Journal of Health Psychology, vol.6, issue.4, pp.405-423, 2001.