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Journal Abstract Search

161 related items for PubMed ID: 10827584

  • 1. Learning about genetic risk. Weighing the risk with the right to know.
    Dorinzi D.
    AWHONN Lifelines; 1999; 3(5):49-52. PubMed ID: 10827584
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  • 7. Utility and limitations of genetic testing and information.
    Bradley AN.
    Nurs Stand; 1999; 20(5):52-5. PubMed ID: 16255487
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  • 10. Recommendations for the predictive genetic test in Huntington's disease.
    MacLeod R, Tibben A, Frontali M, Evers-Kiebooms G, Jones A, Martinez-Descales A, Roos RA, Editorial Committee and Working Group ‘Genetic Testing Counselling’ of the European Huntington Disease Network.
    Clin Genet; 2013 Mar; 83(3):221-31. PubMed ID: 22642570
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  • 11. Prenatal testing for Huntington disease.
    Corson V, Quaid K, Kasch L, Kazazian HH.
    Birth Defects Orig Artic Ser; 1990 Mar; 26(3):226-30. PubMed ID: 2151181
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  • 12. The autonomy paradox: predictive genetic testing and autonomy: three essential problems.
    Huibers AK, van 't Spijker A.
    Patient Educ Couns; 1998 Sep; 35(1):53-62. PubMed ID: 9832897
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  • 15. Genetic markers and the majority's right not to know.
    Appel J, Friedman JH.
    Mov Disord; 2004 Jan; 19(1):113-4. PubMed ID: 14743372
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  • 17. The genetic testing process: how much counseling is needed?
    Cummings S.
    J Clin Oncol; 2000 Nov 01; 18(21 Suppl):60S-4S. PubMed ID: 11060329
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  • 19. The benefits and potential harms of genetic testing for Huntington's disease: a case study.
    Edge K.
    Hum Reprod Genet Ethics; 2008 Nov 01; 14(2):14-9. PubMed ID: 19024332
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