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Results 1 - 1 of 1 for "Beckwith-Wiedemann" syndrome due to CDKN1C mutation
Did you mean "Beckwith-Wiedemann" syndrome due to cdkn2a mutation?
  1. CDKN1C gene 
    ... deletions disrupt the activity of several genes, including CDKN1C.Beckwith-Wiedemann syndrome can also result from variants (also known as mutations) within the maternally inherited copy of the CDKN1C ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics