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

ABSTRACT:

SUBMITTER: Bastaki F 

PROVIDER: S-EPMC4800924 | biostudies-literature | 2016 Feb

REPOSITORIES: biostudies-literature

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

Bastaki Fatma F   Saif Fatima F   Al Ali Mahmoud T MT   Hamzeh Abdul Rezzak AR  

Saudi medical journal 20160201 2

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