Showing results (1-10 of 23) with videos related to
Sort By:
Pageof 3
Journal of Biotechnology|July 20, 2002
The pros and cons of human therapeutic cloning in the public debateIrmgard NippertCommunity Genetics|August 28, 2004
Women's experiences of undergoing BRCA1 and BRCA2 testing: organisation of the German Hereditary Breast and Ovarian Cancer Consortium Survey and Preliminary Data from MünsterIrmgard Nippert, Brigitte Schlegelberger, Community Genetics|September 28, 2006
Education in medical genetics for physicians: GermanyJorg Schmidtke, Yasmin Paul, Irmgard NippertGenetic Testing|April 29, 2005
DNA-based genetic testing is rising steeply in a national health care system with open access to services: a survey of genetic test use in Germany, 1996-2002Jörg Schmidtke, Brigitte Pabst, Irmgard NippertGenes|September 28, 2024
The Role of Patient Organizations in Shaping Research, Health Policies, and Health Services for Rare Genetic Diseases: The Dutch ExperienceYsbrand Poortman, Martina Ens-Dokkum, Irmgard NippertCommunity Genetics|February 13, 2004
40 years later: the health related quality of life of women affected by thalidomideIrmgard Nippert, Birgit Edler, Claudia Schmidt-HerterichGenetic Testing|October 18, 2005
Genotype-based screening for hereditary hemochromatosis: II. Attitudes toward genetic testing and psychosocial impact--a report from a German pilot studyManfred Stuhrmann, Ludwig Hoy, Irmgard Nippert, et al.The American Journal of Bioethics : AJOB|June 5, 2003
In focus. Has patient autonomy gone to far? Geneticists' views in 36 nationsDorothy C Wertz, John C Fletcher, Irmgard Nippert, et al.Community Genetics|January 22, 2008
EuroGentest: DNA-based testing for heritable disorders in EuropePoupak Javaher, Helena Kaariainen, Ulf Kristoffersson, et al.European Journal of Human Genetics : EJHG|May 15, 2008
Regulations and practices of genetic counselling in 38 European countries: the perspective of national representativesElina Rantanen, Marja Hietala, Ulf Kristoffersson, et al.Pageof 3