(Q36417821)

14 August 2017

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title

Guidelines for disclosing genetic information to family members: from development to use. (English)

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14 August 2017

1

Béatrice Godard

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14 August 2017

Thierry Hurlimann

2

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14 August 2017

Martin Letendre

series ordinal

3

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14 August 2017

Nathalie Egalité

series ordinal

4

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14 August 2017

INHERIT BRCAs

series ordinal

5

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14 August 2017

publication date

1 January 2006

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14 August 2017

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14 August 2017

volume

5

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14 August 2017

issue

1

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14 August 2017

page(s)

103-116

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Late onset genetic disease: where ignorance is bliss, is it folly to inform relatives?

14 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10689-005-2581-5

Transmitting genetic risk information in families: attitudes about disclosing the identity of relatives

21 January 2018

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12 December 2020

Response of the law to developments in genetics

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12 December 2020

American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility

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12 December 2020

Guidelines for genetic testing. The Japan Society of Human Genetics, Council Committee of Ethics

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12 December 2020

Genomic torts: the law of the future -- the duty of physicians to disclose the presence of a genetic disease to the relatives of their patients with the disease.

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12 December 2020

In defence of ignorance: genetic information and the right not to know

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12 December 2020

Genetic secrets and the family.

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Communicating genetic test results to the family: a six-step, skills-building strategy

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12 December 2020

Genetic testing and screening: the developing European jurisprudence

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12 December 2020

Familial disclosure in defiance of nonconsent

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12 December 2020

Genetic screening and ethics: European perspectives

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12 December 2020

Is it acceptable to approach colorectal cancer patients at diagnosis to discuss genetic testing? A pilot study

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12 December 2020

Attitudes toward an unsolicited approach in relation to status of genetic disease: exemplified by alpha(1)-antitrypsin deficiency

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12 December 2020

Privacy and disclosure in medical genetics examined in an ethics of care

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12 December 2020

Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients.

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12 December 2020

Genetic links, family ties, and social bonds: rights and responsibilities in the face of genetic knowledge.

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12 December 2020

Convention for the protection of human rights and dignity of the human being with regard to the application of biology and medicine: convention on human rights and biomedicine (adopted by the Committee of Ministers on 19 November 1996). Council of E

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12 December 2020

Confidentiality and serious harm in genetics - preserving the confidentiality of one patient and preventing harm to relatives.

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12 December 2020

ASHG statement. Professional disclosure of familial genetic information. The American Society of Human Genetics Social Issues Subcommittee on Familial Disclosure

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12 December 2020

Notification of a family history of breast cancer: issues of privacy and confidentiality

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12 December 2020

Genetics and assisted procreation. Amendment of Federal Constitution. Dated 13 August 1992. (Recueil officiel des lois fédérales, 25 August 1992, No. 32, pp. 1579-1580)

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12 December 2020

The "duty to warn" a patient's family members about hereditary disease risks

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12 December 2020

Medical Geneticists' duty to warn at-risk relatives for genetic disease

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12 December 2020

Mental disorders and genetics: the ethical context: conclusions and recommendations

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12 December 2020

Genetic professionals' reports of nondisclosure of genetic risk information within families

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12 December 2020

Results of genetic testing: when confidentiality conflicts with a duty to warn relatives

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12 December 2020

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

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12 December 2020

A physician's duty to warn a patient's relatives of a patient's genetically inheritable disease

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12 December 2020

Genetic testing for BRCA1 and BRCA2: recommendations of the Stanford Program in Genomics, Ethics, and Society. Breast Cancer Working Group

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12 December 2020

Patient confidentiality and the surrogate's right to know

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12 December 2020

Disclosure to the family of breast/ovarian cancer genetic test results: patient's willingness and associated factors

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12 December 2020

Duty to warn at‐risk relatives for genetic disease: Genetic counselors' clinical experience

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12 December 2020

Genetic information: a joint account?

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12 December 2020

The evolving duty to disclose the presence of genetic disease to relatives

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12 December 2020

Genetic risk: the new frontier for the duty to warn

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12 December 2020

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

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12 December 2020

Physician's duty to warn third parties about the risk of genetic diseases

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12 December 2020

The legal status of clinical and ethics policies, codes, and guidelines in medical practice and research

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12 December 2020

Genetic information and the family: are we our brother's keeper?

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12 December 2020

Comment on a view favoring ignorance of genetic information: confidentiality, autonomy, beneficence and the right not to know

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12 December 2020

10.1007/S10689-005-2581-5

Identifiers

DOI

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14 August 2017

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