| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Bartha Knoppers | Q2885924 |
| P2093 | author name string | Burgess MM | |
| Laberge CM | |||
| P2860 | cites work | Exploration of the effects of predictive testing for Huntington disease on intimate relationships | Q45307535 |
| Research and stored tissues. Persons as sources, samples as persons? | Q48068522 | ||
| Professional perspectives: a survey of Canadian providers. | Q52019387 | ||
| Multidisciplinary perceptions of human genetics in Canada: "Delphi" results with regards to the practice of medical genetics | Q73201256 | ||
| Regulating NRGTs (new reproductive and genetic technologies): is criminalization the solution for Canada? | Q77155662 | ||
| Bioethics for clinicians: 10. Research ethics | Q34023390 | ||
| Bioethics for clinicians: 8. Confidentiality | Q34038814 | ||
| Structuring the review of human genetics protocols, Part II: diagnostic and screening studies. | Q34412175 | ||
| Bioethics for clinicians: 1. Consent | Q34712602 | ||
| Bioethics for clinicians: 2. Disclosure. | Q34712925 | ||
| Predictive testing for Huntington disease: nonparticipants compared with participants in the Dutch program. | Q35889419 | ||
| Proceed with care: direct predictive testing for Huntington disease. | Q35889463 | ||
| DNA sampling and informed consent | Q39212492 | ||
| Psychological costs and benefits of predictive testing for Huntington's disease | Q39481562 | ||
| Social system responses to Huntington disease | Q44306361 | ||
| Ethical issues in genetic testing for Alzheimer's disease: lessons from Huntington's disease. | Q45289599 | ||
| A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats | Q45289978 | ||
| Genetic testing for Huntington's disease--a family issue | Q45291468 | ||
| Patients' rights to laboratory data: trinucleotide repeat length in Huntington disease | Q45292636 | ||
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | bioethics | Q194294 |
| medical ethics | Q237151 | ||
| research ethics | Q1132684 | ||
| P1104 | number of pages | 5 | |
| P304 | page(s) | 1309-1313 | |
| P577 | publication date | 1998-05-01 | |
| P1433 | published in | Canadian Medical Association Journal | Q5030320 |
| P1476 | title | Bioethics for clinicians: 14. Ethics and genetics in medicine | |
| P478 | volume | 158 |
| Q37881950 | Attitudes of health care professionals toward pharmacogenetic testing |
| Q53414698 | Conflict of interest in medical research in Estonia. |
| Q35537370 | Ethical issues in molecular medicine of relevance to surgeons. |
| Q38609376 | The potential for misusing "genetic predisposition" in Canadian courts and tribunals |
| Q24806160 | The unique ethical challenges of conducting research in the rehabilitation medicine population |
| Q33895354 | The very youngest science |
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