Genetic testing and common disorders in a public health framework: How to assess relevance and possibilities: Background Document to the ESHG recommendations on genetic testing and common disorders

Additional Metadata
Keywords	common disorders, genetic testing, predictive value, monogenic subtypes, public health
Persistent URL	doi.org/10.1038/ejhg.2010.249, hdl.handle.net/1765/23896
Journal	European Journal of Human Genetics
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Becker, F., El, C., Ibarreta, D., Zika, E., Hogarth, S., Borry, P., Cambon-Thomsen, A., Cassiman, J. J., Evers-Kiebooms, G., Hodgson, S., Janssens, C., Kaariainen, H., Krawczak, M., Kristoffersson, U., Lubinski, J., Patch, C., Penchaszadeh, V. B., Read, A., Rogowski, W., … Cornel, M. (2011). Genetic testing and common disorders in a public health framework: How to assess relevance and possibilities: Background Document to the ESHG recommendations on genetic testing and common disorders. European Journal of Human Genetics, 19(SUPPL. 1).https://doi.org/10.1038/ejhg.2010.249

Genetic testing and common disorders in a public health framework: How to assess relevance and possibilities