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.
Full text not available from this repository.
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://eprints.uni-kiel.de/id/eprint/16746 |
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