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Roberta A Pagon University of Washington School of Medicine,
Seattle, WA 98195, USA
Correspondence to: R A Pagon, GeneClinics, Seattle, WA
98115, USA bpagon@u.washington.edu
| The first 150 words of the full text of this article appear below. |
Over the past decade daily advances in gene discovery fuelled by the human genome project have propelled molecular genetic testing into mainstream medicine. Molecular genetic testing is a sensitive, cost effective means of diagnosis, testing for carrier status, and prenatal diagnosis for many inherited disorders, and it is increasingly used for predictive and predispositional testing. Those who rely on genetic testing find it a challenge keeping up to date with information, particularly when guidelines for use lag behind the availability of tests. We looked critically at online resources relevant to geneticists, providers of primary care (who have been identified by their patients as the primary source of information on genetic testing (www.ama-assn.org/ama/pub/article/2304-2937.html)), and informed patients. 1 2
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We relied on our experience as medical geneticist, teachers of
medical students, residents and physicians in internal medicine and
family practice, and medical librarians; our participation in genetics
resources on the web (GROW),
What can you learn from this BMJ paper? Read Leanne Tite's Paper+