Literature DB >> 11645210

Autonomy, respect, and genetic information policy: a reply to Tuija Takala and Matti Häyry.

Rosamond Rhodes.   

Abstract

Keywords:  American Society of Human Genetics; Analytical Approach; Genetics and Reproduction; Professional Patient Relationship

Mesh:

Year:  2000        PMID: 11645210     DOI: 10.1076/0360-5310(200002)25:1;1-V;FT114

Source DB:  PubMed          Journal:  J Med Philos        ISSN: 0360-5310


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  5 in total

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Authors:  Lilian Liou Cohen; Marina Stolerman; Christine Walsh; David Wasserman; Siobhan M Dolan
Journal:  J Med Ethics       Date:  2011-09-27       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.  Communicating genetic information in the family: enriching the debate through the notion of integrity.

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Journal:  Med Health Care Philos       Date:  2008-04-09

4.  Shared decision-making and patient autonomy.

Authors:  Lars Sandman; Christian Munthe
Journal:  Theor Med Bioeth       Date:  2009-08-22

5.  Incidental findings of uncertain significance: To know or not to know--that is not the question.

Authors:  Bjørn Hofmann
Journal:  BMC Med Ethics       Date:  2016-02-13       Impact factor: 2.652

  5 in total

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