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

Samankaltaisia teoksia

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  Julkaistu: (2019)
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• Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome
  Tekijä: Eßinger, Carla, et al.
  Julkaistu: (2020)
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• ZAC, LIT1 (KCNQ1OT1) and p57(KIP2) (CDKN1C) are in an imprinted gene network that may play a role in Beckwith–Wiedemann syndrome
  Tekijä: Arima, Takahiro, et al.
  Julkaistu: (2005)