Molecular and clinical characterization of a nonsense CDKN1C mutation in an Emirati patient with Beckwith-Wiedemann syndrome

Authors

• Fatma Bastaki, From the Department of Pediatrics (Bastaki, Saif), Latifa Hospital, Dubai Health Authority, the Center for Arab Genomic Studies (Al Ali, Hamzeh), Dubai, United Arab Emirates
• Fatima Saif, From the Department of Pediatrics (Bastaki, Saif), Latifa Hospital, Dubai Health Authority, the Center for Arab Genomic Studies (Al Ali, Hamzeh), Dubai, United Arab Emirates
• Abdul Rezzak Hamzeh, From the Department of Pediatrics (Bastaki, Saif), Latifa Hospital, Dubai Health Authority, the Center for Arab Genomic Studies (Al Ali, Hamzeh), Dubai, United Arab Emirates

Article Type

Other

First Page

215

Last Page

216

Recommended Citation

Bastaki, Fatma; Saif, Fatima; and Hamzeh, Abdul Rezzak (2016) "Molecular and clinical characterization of a nonsense CDKN1C mutation in an Emirati patient with Beckwith-Wiedemann syndrome," Saudi Medical Journal: Vol. 37: Iss. 2, Article 18.
DOI: https://doi.org/10.15537/smj.2016.2.13593