Céline Huber and Gheona Altarescu contributed equally to this work.
Article first published online: 3 AUG 2010
Copyright © 2010 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 152A, Issue 9, pages 2230–2235, September 2010
How to Cite
Reish, O., Huber, C., Altarescu, G., Chapman-Shimshoni, D., Levy-Lahad, E., Renbaum, P., Mashevich, M., Munnich, A. and Cormier-Daire, V. (2010), Mosaic compound heterozygosity of SHOX resulting in Leri–Weill dyschondrosteosis with marked short stature: Implications for disease mechanisms and recurrence risks. Am. J. Med. Genet., 152A: 2230–2235. doi: 10.1002/ajmg.a.33563
How to Cite this Article: Reish O, Huber C, Altarescu G, Chapman-Shimshoni D, Levy-Lahad E, Renbaum P, Mashevich M, Munnich A, Cormier-Daire V. 2010. Mosaic compound heterozygosity of SHOX resulting in Leri–Weill dyschondrosteosis with marked short stature: Implications for disease mechanisms and recurrence risks. Am J Med Genet Part A 152A:2230–2235.
- Issue published online: 19 AUG 2010
- Article first published online: 3 AUG 2010
- Manuscript Accepted: 22 MAY 2010
- Manuscript Received: 20 DEC 2009
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