The National Spina Bifida Patient Registry is funded by the National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, grant #1UO1DDD000744.01.
Article first published online: 2 NOV 2012
Copyright © 2012 Wiley Periodicals, Inc.
Birth Defects Research Part A: Clinical and Molecular Teratology
Volume 97, Issue 1, pages 36–41, January 2013
How to Cite
Thibadeau, J. K., Ward, E. A., Soe, M. M., Liu, T., Swanson, M., Sawin, K. J., Freeman, K. A., Castillo, H., Rauen, K. and Schechter, M. S. (2013), Testing the feasibility of a National Spina Bifida Patient Registry . Birth Defects Research Part A: Clinical and Molecular Teratology, 97: 36–41. doi: 10.1002/bdra.23094
The authors have no conflicts of interest to report.
The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.
- Issue published online: 10 JAN 2013
- Article first published online: 2 NOV 2012
- Manuscript Accepted: 25 SEP 2012
- Manuscript Revised: 21 SEP 2012
- Manuscript Received: 3 MAY 2012
Additional Supporting Information may be found in the online version of this article.
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|BDRA_23094_sm_SuppTab3a.tif||123K||Supporting Information Table 3a|
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