P.N., K., R., S., N., S., V., R., J., T., & P., L. (2014). A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases.

P.N., Kantaputra, Sittiwangkul R., Sonsuwan N., Romanelli V., Tenorio J., و Lapunzina P. A Novel Mutation in CDKN1C in Sibs With Beckwith-Wiedemann Syndrome and Cleft Palate, Sensorineural Hearing Loss, and Supernumerary Flexion Creases. 2014.

P.N., Kantaputra, et al. A Novel Mutation in CDKN1C in Sibs With Beckwith-Wiedemann Syndrome and Cleft Palate, Sensorineural Hearing Loss, and Supernumerary Flexion Creases. 2014.