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Nr. |
Eintrag |
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1 |
Clarke, Angus:
Genetic counseling, testing, and screening
In: Kuhse, Helga; Singer, Peter, eds. A Companion to Bioethics. 2nd edition. Chichester, UK; Malden, MA: Wiley-Blackwell, 2009: 245-259 |
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2 |
Hirschberg, Irene (Hg.):
ETHISCHE FRAGEN GENETHISCHER BERATUNG: KLINISCHE ERFAHRUNGEN, FORSCHUNGSSTUDIEN UND SOZIALE PERSPEKTIVEN
2009 |
|
3 |
Lo, Bernard:
Ethical issues in genomic medicine
In: Resolving Ethical Dilemmas: A Guide for Clinicians. 4th edition. Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins, 2009: 311-320 |
|
4 |
Mayor, Susan:
NHS must prepare for non-invasive fetal tests [news]
In: BMJ: British Medical Journal, 2009, Vol. 338 (7692), 434 |
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5 |
Betcher, Jeffrey G.:
Quality of Life and Human Difference edited by David Wasserman, Jerome Bickenbach, and Robert Wachbroit [book review]
In: Ethics and Medicine, 2008, Vol. 24 (2), 126-127 |
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6 |
Morrison, Daniel R.:
Making the autonomous client: how genetic counselors construct autonomous subjects
In: Rothman, Barbara Katz; Armstron, Elizabeth Mitchell; Tiger, Rebecca, eds. Bioethical Issues, Sociological Perspectives. Amsterdam; London: Elsevier JAI, 2008: 179-198 |
|
7 |
Nusbaum, Rachel et al.:
A qualitative description of receiving a diagnosis of clefting in the prenatal or postnatal period
In: Journal of Genetic Counseling, 2008, Vol. 17 (4), 336-350 |
|
8 |
Tóth, Adél; Nyári, Tibor; Szabó, János:
Changing views on the goal of reproductive genetic counselling in Hungary.
In: European Journal of Obstetrics, Gynecology, and Reproductive Biology, 2008, Vol. 137 (1), 3-9 |
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9 |
Zuckerman, S. et al.:
Attitudes of couples identified through screening as carriers of Gaucher disease type 1.
In: Clinical Genetics, 2008, Vol. 74 (6), 566-570 |
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10 |
Clarke, Angus:
Genetic counselling
In: Ashcroft, Richard E.; Dawson, Angus; Draper, Heather; McMillan, John R., eds. Principles of Health Care Ethics. 2nd edition. Chichester, West Sussex, UK; Hoboken, NJ: John Wiley and Sons, 2007: 427-434 |
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11 |
Forrest, Laura E. et al.:
Communicating genetic information in families--a review of guidelines and position papers.
In: European Journal of Human Genetics, 2007, Vol. 15 (6), 612-618 |
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12 |
Ghosh, Kanjaksha; Ghosh, Kinjalka:
Microarray genetic screening: the other side of the coin [letter]
In: Lancet, 2007, Vol. 369 (9566), 992 |
|
13 |
Shevell, Michael I.:
"Eugenics" by another name? [commentary]
In: Canadian Journal of Neurological Sciences = Le Journal Canadien des Sciences Neurologiques, 2007, Vol. 34 (4), 494-495 |
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14 |
Smith, Scott D.:
It's in the genes: as genetic testing gives more clues about who is at risk for disease, the need for genetic counselors grows
In: Minnesota Medicine, 2007, Vol. 90 (5), 10-11 |
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15 |
White, Mary Terrell:
Uncertainty and moral judgment: the limits of reason in genetic decision making
In: Journal of Clinical Ethics, 2007, Vol. 18 (2), 148-155 |
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16 |
Kuehn, Bridget M.:
Study downgrades amniocentesis risk
In: JAMA: The Journal of the American Medical Association, 2006, Vol. 296 (22), 2663-2664 |
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17 |
Lalor, Joan; Begley, Cecily:
Fetal anomaly screening: what do women want to know?
In: Journal of Advanced Nursing, 2006, Vol. 55 (1), 11-19 |
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18 |
Resta, Robert G.:
Defining and redefining the scope and goals of genetic counseling
In: American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2006, Vol. 142 (4), 269-275 |
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19 |
Shiloh, Shoshana; Gerad, Liora; Goldman, Boleslav:
The facilitating role of information provided in genetic counseling for counselees' decisions
In: Genetics in Medicine, 2006, Vol. 8 (2), 116-124 |
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20 |
Stemerding, Dirk; Nelis, Annemiek:
Cancer genetics and its "different faces of autonomy"
In: New Genetics and Society, 2006, Vol. 25 (1), 1-19 |
