Dissemination of information: This case has been entered on Decipher database under the reference number SMH250275.
Article first published online: 13 MAY 2011
Copyright © 2011 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 155, Issue 6, pages 1453–1457, June 2011
How to Cite
Banka, S., Fitzgibbon, G. J., Gaunt, L., Rankin, W. J. and Clayton-Smith, J. (2011), A novel 800 kb microduplication of chromosome 16q22.1 resulting in learning disability and epilepsy may explain phenotypic variability in a family with 15q13 microdeletion. Am. J. Med. Genet., 155: 1453–1457. doi: 10.1002/ajmg.a.34034
How to Cite this Article: Banka S, Fitzgibbon GJ, Gaunt L, Rankin WJ, Clayton-Smith J. 2011. A novel 800 kb microduplication of chromosome 16q22.1 resulting in learning disability and epilepsy may explain phenotypic variability in a family with 15q13 microdeletion. Am J Med Genet Part A 155:1453–1457.
- Issue published online: 20 MAY 2011
- Article first published online: 13 MAY 2011
- Manuscript Accepted: 20 MAR 2011
- Manuscript Received: 4 JAN 2011
- Manchester NIHR Biomedical Research Centre
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