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Community Genetics|April 1, 2008
Participant characteristics that influence consent for genetic research in a population-based survey: the Baltimore epidemiologic catchment area follow-upBriana Mezuk, William W Eaton, Peter ZandiCommunity Genetics|January 17, 2008
'I'm Happy if I Can Help'. Public views on future medicines and gene-based therapy in IcelandJanine M Traulsen, Ingunn Bjornsdóttir, Anna Birna AlmarsdóttirCommunity Genetics|January 17, 2008
Parental Opinions about the Expansion of the Neonatal Screening ProgrammeSymone Detmar, Nynke Dijkstra, Niels Nijsingh, et al.Community Genetics|January 17, 2008
The public's attitudes towards the use of genetic information for medical purposes and its related factors in JapanWakaha IkedaCommunity Genetics|January 17, 2008
Diagnosis of familial hypercholesterolemia in general practice using clinical diagnostic criteria or genetic testing as part of cascade genetic screeningTrond P Leren, Tora Himle Finborud, Turid E Manshaus, et al.Community Genetics|June 5, 2004
Strengthening genetic services in primary care for Asian Americans and Pacific IslandersR GeorgeCommunity Genetics|October 16, 2003
Economic considerations for health insurance coverage of emerging genetic testsMita Giacomini, Fiona Miller, Bernie J O'BrienCommunity Genetics|July 11, 2002
Detection of Congenital Anomalies by Fetal Ultrasonographic Examination across EuropeC. Stoll, R. Tenconi, M. ClementiCommunity Genetics|July 11, 2002
The Opinions, Expectations and Experiences of Women with a Family History of Breast Cancer Who Consult Their GP and Are Referred to Secondary CareA.A.J. Andermann, E.K. Watson, A.M. Lucassen, et al.Community Genetics|August 9, 2001
Finnish physicians' interest in genetic screeningH Toiviainen, E HemminkiPageof 32