A De Novo Deletion at 16q24.3 Involving ANKRD11 in a Japanese Patient With KBG Syndrome
Article first published online: 5 MAR 2013
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 5, pages 1073–1077, May 2013
How to Cite
2012. A de novo deletion at 16q24.3 involving ANKRD11 in a Japanese patient with KBG syndrome. Am J Med Genet Part A 161A:1073–1077., , , , , , .
- Issue published online: 22 APR 2013
- Article first published online: 5 MAR 2013
- Manuscript Accepted: 24 AUG 2012
- Manuscript Received: 28 MAR 2012
- Ministry of Health, Labour, and Welfare of Japan
- Japan Science and Technology Agency
- Ministry of Education, Culture, Sports, Science, and Technology of Japan
- Japan Society for the Promotion of Science
- Yokohama City University
- Japan Epilepsy Research Foundation
- Takeda Science Foundation
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