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9. Ethical and social issues in presymptomatic testing for Huntington's disease: a European Community collaborative study. European Community Huntington's Disease Collaborative Study Group. J Med Genet; 1993 Dec; 30(12):1028-35. PubMed ID: 8133502 [Abstract] [Full Text] [Related]
11. Objective knowledge about Huntington's disease and attitudes towards predictive tests of persons at risk. Teltscher B, Polgar S. J Med Genet; 1981 Feb; 18(1):31-9. PubMed ID: 6454786 [Abstract] [Full Text] [Related]
13. Ethical issues policy statement on Huntington's disease molecular genetics predictive test. International Huntington Association. World Federation of Neurology. Went L. J Med Genet; 1990 Jan; 27(1):34-8. PubMed ID: 2137881 [No Abstract] [Full Text] [Related]
16. World Federation of Neurology: Research Committee. Research Group on Huntington's chorea. Ethical issues policy statement on Huntington's disease molecular genetics predictive test. J Neurol Sci; 1989 Dec; 94(1-3):327-32. PubMed ID: 2533250 [No Abstract] [Full Text] [Related]
17. Huntington's disease predictive testing: the case for an assessment approach to requests from adolescents. Binedell J, Soldan JR, Scourfield J, Harper PS. J Med Genet; 1996 Nov; 33(11):912-8. PubMed ID: 8950670 [Abstract] [Full Text] [Related]
18. To test or not to test: an ethical conflict with presymptomatic testing of individuals at 25% risk for Huntington's disorder. Lindblad AN. Clin Genet; 2001 Dec; 60(6):442-6. PubMed ID: 11846736 [Abstract] [Full Text] [Related]