The authors declare no conflict of interest.
SOCIAL AND BEHAVIOURAL RESEARCH IN CLINICAL GENETICS
Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients
Version of Record online: 4 NOV 2013
© 2013 The Authors. Clinical Genetics published by JohnWiley & Sons A/S. Published by John Wiley & Sons Ltd.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Volume 85, Issue 5, pages 417–422, May 2014
How to Cite
Rigter, T., van Aart, C.J.A., Elting, M.W., Waisfisz, Q., Cornel, M.C. and Henneman, L. (2014), Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients. Clinical Genetics, 85: 417–422. doi: 10.1111/cge.12299
- Issue online: 1 APR 2014
- Version of Record online: 4 NOV 2013
- Accepted manuscript online: 11 OCT 2013 12:54PM EST
- Manuscript Revised: 9 OCT 2013
- Manuscript Accepted: 9 OCT 2013
- Manuscript Received: 28 AUG 2013
- European Commission. Grant Number: HEALTH-F4-2010-261469
- CSG Centre for Society and the Life Sciences
|cge12299-sup-0001-FigureS1.doc||Word document||28K||Fig. S1. Part of the consent form for exome sequencing in clinical diagnostics, VU University Medical Center Amsterdam, March 2012.|
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