Frank Rutsch and Raoul C.M. Hennekam contributed equally to this study.
Version of Record online: 15 JAN 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 2, pages 360–370, February 2013
How to Cite
Feigenbaum, A., Müller, C., Yale, C., Kleinheinz, J., Jezewski, P., Kehl, H. G., MacDougall, M., Rutsch, F. and Hennekam, R. C.M. (2013), Singleton–Merten syndrome: An autosomal dominant disorder with variable expression. Am. J. Med. Genet., 161: 360–370. doi: 10.1002/ajmg.a.35732
How to Cite this Article: Feigenbaum A, Müller C, Yale C, Kleinheinz J, Jezewski P, Kehl HG, MacDougall M, Rutsch F, Hennekam RCM. 2013. Singleton–Merten syndrome: An autosomal dominant disorder with variable expression. Am J Med Genet Part A 161A:360–370.
- Issue online: 24 JAN 2013
- Version of Record online: 15 JAN 2013
- Manuscript Accepted: 14 SEP 2012
- Manuscript Received: 26 JUN 2012
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