|
Nr. |
Eintrag |
|
1 |
Bartens, Werner:
Das Dilemma der Diagnose : Ärzte formulieren komplexe Befunde, doch mit dem subjektiven Erleben der Patienten hat das oft nichts zu tun. Wer bei der Knieuntersuchung ein bisschen aufgeregt ist, riskiert fortan, gegen Bluthochdruck behandelt zu werden
In: Süddeutsche Zeitung, 2015 (2015-06-26) |
|
2 |
Schäfer, Susanne:
Das Gesundheits-Orakel : Mit Analysen von Speichel, Blut und Urin kann sich jetzt jeder zu Hause selber überwachen - und sich von den Ergebnissen erschrecken lassen. Dabei sind nicht alle Tests sinnvoll
In: Die Zeit, 2015 (2015-12-17) |
|
3 |
Appleby, Julie:
Hospitals promote screenings that experts say many people do not need
In: Washington Post, 2013 (2013-05-13) |
|
4 |
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 |
|
5 |
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 |
|
6 |
Hobson, Katherine:
The power of tracing your medical roots
In: U.S. News and World Report, 2009, Vol. 146 (11), 83-84 |
|
7 |
Malone, F:
Implications of noninvasive prenatal diagnosis.
In: Irish medical journal, 2009, Vol. 102 (9), 277-8 |
|
8 |
Agence de la biomedecine:
Etat des lieux du diagnostic prénatal en France
2008 |
|
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 |
|
11 |
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 |
|
12 |
Yamanouchi, Y. et al.:
Clinical genetics and general physician: attitude survey [abstract]
In: Journal of Genetic Counseling, 2008, Vol. 17 (6), 645 |
|
13 |
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 |
|
14 |
Biesecker, B. et al.:
Decision-making for invasive prenatal testing: the role of ambivalence
In: Journal of Genetic Counseling, 2007, Vol. 16 (6), 682 |
|
15 |
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 |
|
16 |
Ghosh, Kanjaksha; Ghosh, Kinjalka:
Microarray genetic screening: the other side of the coin [letter]
In: Lancet, 2007, Vol. 369 (9566), 992 |
|
17 |
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 |
|
18 |
Prenatal genetic screening [news brief]
In: CMAJ/JAMC: Canadian Medical Association Journal, 2007, Vol. 176 (8), 1074 |
|
19 |
Godeau, P; Couturier, D:
La diagnostic en médecine : histoire, mise en oeuvre présente, perspectives. Rapport au nom d'un groupe de travail
In: Bulletin de l'Académie nationale de médecine, 2006, Vol. 190 (7), 1533-1550 |
|
20 |
Kuehn, Bridget M.:
Study downgrades amniocentesis risk
In: JAMA: The Journal of the American Medical Association, 2006, Vol. 296 (22), 2663-2664 |
