A Rare Disease Patient Manager
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-28839-5_20.pdf
Reference17 articles.
1. Nabarette, H., Oziel, D., Urbero, B., Maxime, N., Aymé, S.: Use of a directory of specialized services and guidance in the healthcare system: the example of the Orphanet database for rare diseases. Revue d’épidémiologie et de santé publique 54(1), 41 (2006)
2. Schieppati, A., Henter, J.I., Daina, E., Aperia, A.: Why rare diseases are an important medical and social issue. The Lancet 371(9629), 2039–2041 (2008)
3. Burke, W.: Genetic testing. N. Engl. J. Med. 347(23), 1867–1875 (2002)
4. Krawczak, M., Ball, E.V., Fenton, I., Stenson, P.D., Abeysinghe, S., Thomas, N., Cooper, D.N.: Human gene mutation database—a biomedical information and research resource. Human Mutation 15(1), 45–51 (2000)
5. Via, M., Gignoux, C., Burchard, E.G.: The 1000 Genomes Project: new opportunities for research and social challenges. Genome Medicine 2(1), 1–3 (2010)
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