How to Cite this Article: Kantaputra PN, Sittiwangkul R, Sonsuwan N, Romanelli V, Tenorio J, Lapunzina P. 2012. A novel mutation in CDKN1C in sibs with Beckwith–Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases. Am J Med Genet Part A 161A:192–197.
Version of Record online: 29 NOV 2012
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 1, pages 192–197, January 2013
How to Cite
Kantaputra, P. N., Sittiwangkul, R., Sonsuwan, N., Romanelli, V., Tenorio, J. and Lapunzina, P. (2013), A novel mutation in CDKN1C in sibs with Beckwith–Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases. Am. J. Med. Genet., 161: 192–197. doi: 10.1002/ajmg.a.35663
Conflict of interest: none to delcare.
- Issue online: 22 DEC 2012
- Version of Record online: 29 NOV 2012
- Manuscript Accepted: 24 AUG 2012
- Manuscript Received: 15 MAR 2012
- Thailand Research Fund
- Faculty of Dentistry, Chiang Mai ISCIII-FIS 11/2491 (PL)
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