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Nr. |
Eintrag |
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1 |
Becker, Frauke et al.:
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders.
In: European journal of human genetics : EJHG 2011 Apr; 19 Suppl 1: S6-44 |
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2 |
Bunnik, Eline M; Schermer, Maartje H N; Janssens, A Cecile J W:
Personal genome testing: test characteristics to clarify the discourse on ethical, legal and societal issues.
In: BMC medical ethics, 2011, 12, 11 |
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3 |
Nau, Jean-Yves:
[Genetic entertainment and coffee grounds]. = "Génétique récréative" et marc de café.
In: Revue médicale suisse, 2011, Vol. 7 (303), 1518-9 |
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4 |
ACOEM Task Force on Genetic Screening in the Workplace:
Genetic screening in the workplace.
In: Journal of occupational and environmental medicine / American College of Occupational and Environmental Medicine, 2010, Vol. 52 (7), 763 |
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5 |
Black, Lee; Simard, Jacques; Knoppers, Bartha Maria:
Genetic testing, physicians and the law: will the tortoise ever catch up with the hare?
In: Annals of health law / Loyola University Chicago, School of Law, Institute for Health Law, 2010, Vol. 19 (1 Spec No), 115-20 |
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6 |
Burke, Wylie; Laberge, A.-M.; Press, N.:
Debating clinical utility.
In: Public Health Genomics, 2010, Vol. 13 (4), 215-223 |
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7 |
Caulfield, T. et al.:
Direct-to-consumer genetic testing: good, bad or benign?
In: Clinical Genetics, 2010, Vol. 77 (2), 101-105 |
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8 |
Couzin-Frankel, Jennifer:
Chasing a disease to the vanishing point. Genetic testing is making a rare disease, familial dysautonomia, ever rarer. At the same time, more tools than ever are available to study it.
In: Science, 2010, Vol. 328 (5976), 298-300 |
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9 |
Evans, James P:
Putting patients before patents.
In: Genetics in medicine : official journal of the American College of Medical Genetics 2010 Apr ; 12(4): 204-5 |
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10 |
Javaher, P et al.:
Genetic screening in Europe.
In: Public health genomics, 2010, Vol. 13 (7-8), 524-37 |
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11 |
Matsuda, Ichiro:
[Ethical, legal and social implication of genetic testing].
In: Nippon rinsho. Japanese journal of clinical medicine 2010 Aug; 68 Suppl 8: 294-8 |
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12 |
Pàmpols Ros, Teresa et al.:
[The ethical aspects of population screening programme of rare diseases]. = Recomendaciones sobre los aspectos éticos de los programas de cribado de población para enfermedades raras.
In: Revista española de salud pública, 2010, Vol. 84 (2), 121-36 |
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13 |
Tamir, Sivan:
Direct-to-consumer genetic testing: ethical-legal perspectives and practical considerations.
In: Medical law review, 2010, Vol. 18 (2), 213-38 |
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14 |
Wagner, Jennifer K:
Interpreting the implications of DNA ancestry tests.
In: Perspectives in biology and medicine, 2010, Vol. 53 (2), 231-48 |
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15 |
Buchanan, Janet A. et al.:
The cycle of genome-directed medicine.
In: Genome Medicine, 2009, Vol. 1 (2), 16 |
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16 |
Groopman, Jerome; Hartzband, Pamela:
What's your underlying condition? [op-ed]
In: New York Times, 2009 (2009-11-27), A39 |
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17 |
Reynolds, Timothy M:
The ethics of antenatal screening: lessons from Canute.
In: The Clinical biochemist. Reviews / Australian Association of Clinical Biochemists 2009 Nov ; 30(4): 187-96 |
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18 |
Romeo Casabona, Carlos Maria:
Predictivity, genetic tests and insurance law.
In: Law and the human genome review = Revista de derecho y genoma humano / Chair in Law and the Human Genome, BBV Foundation-Provincial Government of Biscay, University of Deusto 2009 Jul-Dec(31): 107-22 |
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19 |
Zeiler, Kristin:
Symposium on genetics, identity, and ethics [editorial]
In: New Genetics and Society, 2009, Vol. 28 (2), 153-156 |
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20 |
Feroni, I et al.:
Incertitudes et décisions en médecine (dossier)
In: In: Sciences sociales et santé
2008 |
