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Nr. |
Eintrag |
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1 |
Hall, Alison; Bostanci, A.; Wright, C.F.:
Non-invasive prenatal diagnosis using cell-free fetal DNA technology: applications and implications.
In: Public Health Genomics, 2010, Vol. 13 (4), 246-255 |
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2 |
Hirschberg, Irene (Hg.):
ETHISCHE FRAGEN GENETHISCHER BERATUNG: KLINISCHE ERFAHRUNGEN, FORSCHUNGSSTUDIEN UND SOZIALE PERSPEKTIVEN
2009 |
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3 |
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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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 |
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 |
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6 |
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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7 |
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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8 |
Aalfs, C.M.; Smets, E.M.A.; Leschot, N.J.:
Genetic counselling for familial conditions during pregnancy: a review of the literature published during the years 1989-2004
In: Community Genetics, 2007, Vol. 10 (3), 159-168 |
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9 |
Atkins, Loren:
Defending the Genetic Supermarket
In: University of Tasmania Law Review, 2007, Vol. 26 (2), 206-208 |
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10 |
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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11 |
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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12 |
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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13 |
Ghosh, Kanjaksha; Ghosh, Kinjalka:
Microarray genetic screening: the other side of the coin [letter]
In: Lancet, 2007, Vol. 369 (9566), 992 |
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14 |
Hodgson, J.:
Testing times, challenging choices: women, prenatal testing and genetic counseling
In: Journal of Genetic Counseling, 2007, Vol. 16 (6), 685 |
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15 |
Kalokairinou, E.M.:
The experience of ß-thalassaemia and its prevention in Cyprus
In: Medicine and Law: The World Association for Medical Law, 2007, Vol. 26 (2), 291-307 |
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16 |
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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17 |
Prenatal genetic screening [news brief]
In: CMAJ/JAMC: Canadian Medical Association Journal, 2007, Vol. 176 (8), 1074 |
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18 |
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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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 |
Al-Gazali, L.I.:
Attitudes toward genetic counseling in the United Arab Emirates
In: Community Genetics, 2005, Vol. 8 (1), 48-51 |
