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Molecular and clinical characterization of a nonsense CDKN1C mutation in an Emirati patient with Beckwith-Wiedemann syndrome
Fatma Bastaki, Fatima Saif, Mahmoud T. Al Ali and Abdul Rezzak Hamzeh
Saudi Medical Journal February 2016, 37 (2) 215-216; DOI: https://doi.org/10.15537/smj.2016.2.13593
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
MD, CGFatima 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
MD, PDMahmoud T. Al Ali
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
BSc, PhDAbdul 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
BPharm, PhD
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Molecular and clinical characterization of a nonsense CDKN1C mutation in an Emirati patient with Beckwith-Wiedemann syndrome
Fatma Bastaki, Fatima Saif, Mahmoud T. Al Ali, Abdul Rezzak Hamzeh
Saudi Medical Journal Feb 2016, 37 (2) 215-216; DOI: 10.15537/smj.2016.2.13593
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