Literature DB >> 11789514

Protecting and promoting privacy in an uncertain world: further defences of ignorance and the right not to know.

G T Laurie1.   

Abstract

Keywords:  Genetics and Reproduction; Professional Patient Relationship

Mesh：

Year:  2000        PMID： 11789514     DOI： 10.1163/15718090020523142

Source DB:  PubMed          Journal:  Eur J Health Law        ISSN： 0929-0273


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  7 in total

1.  Genetic testing without consent: the implications of the new Human Tissue Act 2004.

Authors:  A Lucassen; J Kaye
Journal:  J Med Ethics       Date:  2006-12       Impact factor: 2.903

2.  Questioning the consensus: managing carrier status results generated by newborn screening.

Authors:  Fiona Alice Miller; Jason Scott Robert; Robin Z Hayeems
Journal:  Am J Public Health       Date:  2008-12-04       Impact factor: 9.308

3.  Decision-making about inherited cancer risk: exploring dimensions of genetic responsibility.

Authors:  Holly Etchegary; Fiona Miller; Sonya deLaat; Brenda Wilson; June Carroll; Mario Cappelli
Journal:  J Genet Couns       Date:  2009-03-18       Impact factor: 2.537

4.  Consent to epistemic interventions: a contribution to the debate on the right (not) to know.

Authors:  Niels Nijsingh
Journal:  Med Health Care Philos       Date:  2016-03

5.  The right not to know: an autonomy based approach.

Authors:  R Andorno
Journal:  J Med Ethics       Date:  2004-10       Impact factor: 2.903

Review 6.  Guidelines for disclosing genetic information to family members: from development to use.

Authors:  Béatrice Godard; Thierry Hurlimann; Martin Letendre; Nathalie Egalité
Journal:  Fam Cancer       Date:  2006       Impact factor: 2.375

Review 7.  Ignorance, information and autonomy.

Authors:  J Harris; K Keywood
Journal:  Theor Med Bioeth       Date:  2001-09
  7 in total

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