-
1
-
-
6444221054
-
The right not to know: an autonomy based approach
-
Andorno, Roberto (2004) The right not to know: an autonomy based approach. Journal of Medical Ethics 29: 435-439.
-
(2004)
Journal of Medical Ethics
, vol.29
, pp. 435-439
-
-
Roberto, A.1
-
2
-
-
0003994619
-
-
Chicago/London: University of Chicago Press
-
Bloor, David (1976) Knowledge and Social Imagery. Chicago/London: University of Chicago Press.
-
(1976)
Knowledge and Social Imagery
-
-
David, B.1
-
3
-
-
84888127976
-
The relative importance of undesirable truths
-
Bortolotti, Lisa (2013) The relative importance of undesirable truths. Medicine, Health Care and Philosophy 16: 683-690.
-
(2013)
Medicine, Health Care and Philosophy
, vol.16
, pp. 683-690
-
-
Lisa, B.1
-
4
-
-
79956120702
-
Is there a duty to remain in ignorance?
-
Brassington, Iain (2011) Is there a duty to remain in ignorance? Theoretical Medicine and Bioethics 32: 101-115.
-
(2011)
Theoretical Medicine and Bioethics
, vol.32
, pp. 101-115
-
-
Iain, B.1
-
5
-
-
79952910488
-
The right to know and the right not to know - ten years on
-
Christoph Rehmann-Sutter/Hansjakob Müller (eds.),Farnham, UK/Burlington, VT: Ashgate
-
Chadwick, Ruth (2009) The right to know and the right not to know - ten years on. In Christoph Rehmann-Sutter/Hansjakob Müller (eds.) Disclosure Dilemmas: Ethics of Genetic Prognosis after the "Right to Know/Not to Know", Debate. Farnham, UK/Burlington, VT: Ashgate, 9-19.
-
(2009)
Disclosure Dilemmas: Ethics of Genetic Prognosis after the "Right to Know/Not to Know", Debate
, pp. 9-19
-
-
Ruth, C.1
-
7
-
-
0035677057
-
Ignorance, information and autonomy
-
Harris, John and Keywood, Kirsty (2001) Ignorance, information and autonomy. Theoretical Medicine 22: 415-436.
-
(2001)
Theoretical Medicine
, vol.22
, pp. 415-436
-
-
John, H.1
Kirsty, K.2
-
8
-
-
0035673104
-
Genetic information, rights, and autonomy
-
Häyry, Matti and Takala, Tuija (2001) Genetic information, rights, and autonomy. Theoretical Medicine 22: 403-414.
-
(2001)
Theoretical Medicine
, vol.22
, pp. 403-414
-
-
Matti, H.1
Tuija, T.2
-
11
-
-
0001999169
-
Autonomy and the right not to know
-
Ruth Chadwick, Mairi Levitt and Darren Shickle (eds.),Aldershot, UK: Avebury
-
Husted, Jørgen (1997) Autonomy and the right not to know. In Ruth Chadwick, Mairi Levitt and Darren Shickle (eds.) The Right to Know and the Right Not to Know. Aldershot, UK: Avebury, 55-68.
-
(1997)
The Right to Know and the Right Not to Know
, pp. 55-68
-
-
Jørgen, H.1
-
13
-
-
58849153345
-
Choosing not to choose: reproductive responses of parents of children with genetic conditions or impairments
-
Kelly, Susan (2009) Choosing not to choose: reproductive responses of parents of children with genetic conditions or impairments. Sociology of Health & Illness 31: 81-97.
-
(2009)
Sociology of Health & Illness
, vol.31
, pp. 81-97
-
-
Susan, K.1
-
14
-
-
84867475619
-
Comprehensive carrier screening and molecular diagnostic testing for recessive childhood diseases
-
2012 May 2. Edition 1. doi:
-
Kingsmore, Stephen (2012) Comprehensive carrier screening and molecular diagnostic testing for recessive childhood diseases. PLOS Currents, Evidence on Genomic Tests, 2012 May 2. Edition 1. doi: 10.1371/4f9877ab8ffa9.
-
(2012)
PLOS Currents, Evidence on Genomic Tests
-
-
Stephen, K.1
-
16
-
-
0032791784
-
In defense of ignorance: genetic information and the right not to know
-
Laurie, Graeme T. (1999) In defense of ignorance: genetic information and the right not to know. European Journal of Health Law 6: 119-132.
-
(1999)
European Journal of Health Law
, vol.6
, pp. 119-132
-
-
Graeme, L.T.1
-
18
-
-
84961254354
-
Testing for susceptibility genes: a cautionary tale
-
Christoph Rehmann-Sutter/ Hansjakob Müller (eds.),Farnham, UK/Burlington, VT: Ashgate
-
Lock, Margaret (2009) Testing for susceptibility genes: a cautionary tale. In Christoph Rehmann-Sutter/ Hansjakob Müller (eds.) Disclosure Dilemmas: Ethics of Genetic Prognosis after the "Right to Know/Not to Know" Debate. Farnham, UK/Burlington, VT: Ashgate, 65-83.
-
(2009)
Disclosure Dilemmas: Ethics of Genetic Prognosis after the "Right to Know/Not to Know" Debate
, pp. 65-83
-
-
Margaret, L.1
-
20
-
-
79952233806
-
Enacting genetic responsibility: experiences of mothers who carry the fragile X gene
-
Raspberry, Kelly and Skinner, Debra (2011) Enacting genetic responsibility: experiences of mothers who carry the fragile X gene. Sociology of Health & Illness 33: 420-433.
-
(2011)
Sociology of Health & Illness
, vol.33
, pp. 420-433
-
-
Kelly, R.1
Debra, S.2
-
21
-
-
33847043917
-
To know or not to know: a review of behaviour and suicidal ideation in preclinical Huntington's disease
-
Robins-Wahlin, Tarja-Brita (2007) To know or not to know: a review of behaviour and suicidal ideation in preclinical Huntington's disease. Patient Education and Counseling 65: 279-287.
-
(2007)
Patient Education and Counseling
, vol.65
, pp. 279-287
-
-
Tarja-Brita, R.-W.1
|