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3. Patient autonomy and value-neutrality in nondirective genetic counseling. Wachbroit R; Wasserman D Stanford Law Pol Rev; 1995; 6(2):103-11. PubMed ID: 11660658 [No Abstract] [Full Text] [Related]
4. Genetic testing: is there a right not to know? Rhodes R MCN Am J Matern Child Nurs; 2006; 31(3):145. PubMed ID: 16679953 [No Abstract] [Full Text] [Related]
5. Genetic testing: is there a right not to know? Zinberg RE MCN Am J Matern Child Nurs; 2006; 31(3):144. PubMed ID: 16679952 [No Abstract] [Full Text] [Related]
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8. Genetic information, rights, and autonomy. Häyry M; Takala T Theor Med Bioeth; 2001 Sep; 22(5):403-14. PubMed ID: 11808676 [TBL] [Abstract][Full Text] [Related]
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15. Choices and rights: eugenics, genetics and disability equality. Shakespeare T Disabil Soc; 1998 Nov; 13(5):665-81. PubMed ID: 11660717 [No Abstract] [Full Text] [Related]
16. [Ethical deliberations on genetic testing in children and adolescents]. Esquerda M; Gabaldón S; Gean E; Rev Neurol; 2013 Sep; 57(5):237-9. PubMed ID: 23975531 [No Abstract] [Full Text] [Related]
17. Ethical questions in the age of the new eugenics. Wiesenthal DL; Wiener NI Sci Eng Ethics; 1999 Jul; 5(3):383-94. PubMed ID: 11657752 [No Abstract] [Full Text] [Related]
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19. Clarifying the goals of nondirective genetic counseling. Wachbroit R; Wasserman D Rep Inst Philos Public Policy; 1995; 15(2-3):1-6. PubMed ID: 11660057 [No Abstract] [Full Text] [Related]
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