Conradi–Hünermann–Happle Syndrome: A Novel Heterozygous Missense Mutation, c.204G>T (p.W68C)
Version of Record online: 11 JUN 2014
© 2014 Wiley Periodicals, Inc.
Volume 31, Issue 4, pages 493–496, July/August 2014
How to Cite
Lambrecht, C., Wouters, C., Van Esch, H., Moens, P., Casteels, I. and Morren, M.-A. (2014), Conradi–Hünermann–Happle Syndrome: A Novel Heterozygous Missense Mutation, c.204G>T (p.W68C). Pediatric Dermatology, 31: 493–496. doi: 10.1111/pde.12336
- Issue online: 14 JUL 2014
- Version of Record online: 11 JUN 2014
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