How to Cite this Article: Davis LK, Maltman N, Mosconi MW, Macmillan C, Schmitt L, Moore K, Francis SM, Jacob S, Sweeney JA, Cook EH. 2012. Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis. Am J Med Genet Part A. 158A:1654–1661.
Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis†
Version of Record online: 7 JUN 2012
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 158A, Issue 7, pages 1654–1661, July 2012
How to Cite
Davis, L.K., Maltman, N., Mosconi, M.W., Macmillan, C., Schmitt, L., Moore, K., Francis, S.M., Jacob, S., Sweeney, J.A. and Cook, E.H. (2012), Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis. Am. J. Med. Genet., 158A: 1654–1661. doi: 10.1002/ajmg.a.35396
- Issue online: 18 JUN 2012
- Version of Record online: 7 JUN 2012
- Manuscript Accepted: 3 MAR 2012
- Manuscript Received: 26 JUL 2011
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