Conflicts of interest: None.
Version of Record online: 18 JUN 2012
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 158A, Issue 8, pages 1982–1986, August 2012
How to Cite
Asakura, Y., Muroya, K., Sato, T., Kurosawa, K., Nishimura, G. and Adachi, M. (2012), First case of a Japanese girl with Myhre syndrome due to a heterozygous SMAD4 mutation. Am. J. Med. Genet., 158A: 1982–1986. doi: 10.1002/ajmg.a.35440
How to Cite this Article: Asakura Y, Muroya K, Sato T, Kurosawa K, Nishimura G, Adachi M. 2012. First case of a Japanese girl with Myhre syndrome due to a heterozygous SMAD4 mutation. Am J Med Genet Part A. 158A:1982–1986.
- Issue online: 19 JUL 2012
- Version of Record online: 18 JUN 2012
- Manuscript Accepted: 1 APR 2012
- Manuscript Received: 7 MAR 2012
Additional Supporting Information may be found in the online version of this article.
|ajmg_35440_sm_SupplFig1.tif||1811K||eFig. 1: Partial sequences of PCR products of the patient are shown. The arrow indicates the heterozygous substitution of Ile 500 with threonine.|
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