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Nr. |
Eintrag |
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1 |
Alfirevic, Zarko:
Prenatal screening for Down's syndrome: a range of options that provide reliable and reproducible results is essential [editorial]
In: BMJ: British Medical Journal, 2009, Vol. 338 (7692), 421-422 |
|
2 |
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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3 |
Hobson, Katherine:
The diet of the future: geared to your genes
In: U.S. News and World Report, 2009, Vol. 146 (11), 38, 41 |
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4 |
Hobson, Katherine:
The power of tracing your medical roots
In: U.S. News and World Report, 2009, Vol. 146 (11), 83-84 |
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5 |
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 |
|
6 |
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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7 |
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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8 |
Eells, R. et al.:
The current perceptions and desires of adults with Marfan syndrome on preconceptional and prenatal genetic testing [abstract]
In: Journal of Genetic Counseling, 2008, Vol. 17 (6), 592 |
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9 |
Hall, Alison; Bostanci, A.W.S.; John, S.D.:
Ethical, legal and social issues arising from cell free-fatal DNA technologies [abstract; poster 4.05]
In: Journal of Medical Genetics, 2008, Vol. 45 (Supplement 1), S102 |
|
10 |
Hines, K. et al.:
Genetic counselors' perceived responsibilities regarding reproductive issues for patients at risk for Huntington disease [abstract]
In: Journal of Genetic Counseling, 2008, Vol. 17 (6), 611-612 |
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11 |
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 |
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12 |
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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13 |
Yamanouchi, Y. et al.:
Clinical genetics and general physician: attitude survey [abstract]
In: Journal of Genetic Counseling, 2008, Vol. 17 (6), 645 |
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14 |
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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15 |
Atkins, Loren:
Defending the Genetic Supermarket
In: University of Tasmania Law Review, 2007, Vol. 26 (2), 206-208 |
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16 |
Bache, Iben; Brondum-Nielsen, Karen; Tommerup, Niels:
Genetic counseling in adult carriers of a balanced chromosomal rearrangement ascertained in childhood: experiences from a nationwide reexamination of translocation carriers
In: Genetics in Medicine, 2007, Vol. 9 (3), 185-187 |
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17 |
Biesecker, B. et al.:
Decision-making for invasive prenatal testing: the role of ambivalence
In: Journal of Genetic Counseling, 2007, Vol. 16 (6), 682 |
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18 |
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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19 |
Etchegary, Holly; Perrier, Colin:
Information processing in the context of genetic risk: implications for genetic-risk communication
In: Journal of Genetic Counseling, 2007, Vol. 16 (4), 419-432 |
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20 |
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 |
