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.

Becker, F., van El, C. G., Ibarreta, D., Zika, E., Hogarth, S., Borry, P., Cambon-Thomsen, A., Cassiman, J. J., Evers-Kiebooms, G., Hodgson, S., Janssens, Acjw, Kaariainen, H., Krawczak, M., Kristoffersson, U., Lubinski, J., Patch, C., Penchaszadeh, V. B., Read, A., Rogowski, W., Sequeiros, J., Tranebjaerg, L., van Langen, I. M., Wallace, H., Zimmern, R., Schmidtke, J. and Cornel, M. C. (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, 18 . S6-S44. DOI 10.1038/ejhg.2010.249.

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Supplementary data:

Document Type: Article
Keywords: common disorders genetic testing predictive value monogenic subtypes public health cost-effectiveness analysis genome-wide association factor-v-leiden familial adenomatous polyposis nonpolyposis colorectal-carcinoma hereditary hemochromatosis mutation metastatic breast-cancer coronary-artery-disease venous thromboembolism myocardial-infarction
Research affiliation: Kiel University
Refereed: Yes
DOI etc.: 10.1038/ejhg.2010.249
ISSN: 1018-4813
Date Deposited: 01 Nov 2012 05:05
Last Modified: 23 Jan 2013 10:01
URI: http://oceanrep.geomar.de/id/eprint/16746

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