Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: Delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications
Version of Record online: 8 SEP 2005
Copyright © 2005 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 138A, Issue 2, pages 175–180, 1 October 2005
How to Cite
Yatsenko, S. A., Treadwell-Deering, D., Krull, K., Lewis, R. A., Glaze, D., Stankiewicz, P., Lupski, J. R. and Potocki, L. (2005), Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: Delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications. Am. J. Med. Genet., 138A: 175–180. doi: 10.1002/ajmg.a.30948
- Issue online: 16 SEP 2005
- Version of Record online: 8 SEP 2005
- Manuscript Accepted: 30 JUN 2005
- Manuscript Received: 8 MAR 2005
- National Institutes of Health. Grant Number: GCRC (M01RR00188)
- National Institute of Child Health and Human Development. Grant Number: PO1 HD39420
- Baylor College of Medicine Mental Retardation Research Center. Grant Number: HD2406407
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