Funding sources: Some of the work described in this manuscript presents independent research funded by the National Institute for Health Research (NIHR) under the Programme Grants for Applied Research programme (the ‘RAPID’ project) (RP-PG-0707-10107) and the Central and East London NIHR Comprehensive Local Research Network. Professor Lyn S. Chitty is partially funded by the Great Ormond Street Hospital Children's Charity and the NIHR Biomedical Research Centre at Great Ormond Street Hospital. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health.
The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made
Article first published online: 17 MAY 2013
© 2013 John Wiley & Sons, Ltd.
Special Issue: Noninvasive Prenatal Testing Using Maternal Plasma DNA: Part I
Volume 33, Issue 6, pages 555–562, June 2013
How to Cite
Lench, N., Barrett, A., Fielding, S., McKay, F., Hill, M., Jenkins, L., White, H. and Chitty, L. S. (2013), The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made. Prenat. Diagn., 33: 555–562. doi: 10.1002/pd.4124
Conflicts of interest: None declared
- Issue published online: 17 MAY 2013
- Article first published online: 17 MAY 2013
- Accepted manuscript online: 16 APR 2013 08:39AM EST
Supporting information may be found in the online version of this article.
|PD_4124_Supplementary_Table_1.doc||Word document||230K||Supporting Information|
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