Paweł Stankiewicz and Alma Kuechler contributed equally to this work.
Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation†
Article first published online: 6 FEB 2006
Copyright © 2006 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 140A, Issue 5, pages 442–452, 1 March 2006
How to Cite
Stankiewicz, P., Kuechler, A., Eller, C. D., Sahoo, T., Baldermann, C., Lieser, U., Hesse, M., Gläser, C., Hagemann, M., Yatsenko, S. A., Liehr, T., Horsthemke, B., Claussen, U., Marahrens, Y., Lupski, J. R. and Hansmann, I. (2006), Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation. Am. J. Med. Genet., 140A: 442–452. doi: 10.1002/ajmg.a.31096
- Issue published online: 13 FEB 2006
- Article first published online: 6 FEB 2006
- Manuscript Accepted: 9 NOV 2005
- Manuscript Received: 2 JUN 2005
- National Institute of Child Health and Human Development. Grant Numbers: PO1 HD39420, R01HD041451
- National Science Foundation. Grant Number: DGE-9987641
- Mental Retardation Research Center. Grant Number: HD24064
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