(Q45291643)

11 December 2017

title

The benefits and potential harms of genetic testing for Huntington's disease: a case study (English)

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11 December 2017

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Kathryn Edge

1

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11 December 2017

publication date

1 January 2008

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Human Reproduction and Genetic Ethics

11 December 2017

published in

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11 December 2017

volume

14

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11 December 2017

issue

2

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11 December 2017

page(s)

14-19

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Disclosure of Huntington's disease to family members: the dilemma of known but unknowing parties

11 December 2017

cites work

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https://api.crossref.org/works/10.1558%2FHRGE.V14I2.14

High suicidal ideation in persons testing for Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1558%2FHRGE.V14I2.14

Critical periods of suicide risk in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1558%2FHRGE.V14I2.14

Psychological distress in the 5-year period after predictive testing for Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1558%2FHRGE.V14I2.14

Psychological effect of genetic testing for Huntington's disease: an update of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1558%2FHRGE.V14I2.14

Commodification of children again and non-disclosure preimplantation genetic diagnosis for Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1558%2FHRGE.V14I2.14

Individual, family, and societal dimensions of genetic discrimination: a case study analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1558%2FHRGE.V14I2.14

Teacher was refused job because relatives have Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1558%2FHRGE.V14I2.14

21 January 2018

Identifiers

DOI

10.1558/HRGE.V14I2.14

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11 December 2017

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