In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene

Míreanna Comhchosúla

• Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus
  le: Valente, Federica Maria, et al.
  Foilsithe: (2019)
• Genomic imprinting and the Beckwith-Wiedemann syndrome.
  le: Brown, K W, et al.
  Foilsithe: (1990)
• Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome
  le: Eßinger, Carla, et al.
  Foilsithe: (2020)
• Beckwith-Wiedemann syndrome: imprinting in clusters revisited
  le: Maher, Eamonn R., et al.
  Foilsithe: (2000)
• ZAC, LIT1 (KCNQ1OT1) and p57(KIP2) (CDKN1C) are in an imprinted gene network that may play a role in Beckwith–Wiedemann syndrome
  le: Arima, Takahiro, et al.
  Foilsithe: (2005)