Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting…

Overview of attention for article published in Clinical Epigenetics, May 2022

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Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances https://t.co/A9BbcNbSmU https://t.co/HpihvjO7TA

18 Jun 2022

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RT @ManelEsteller: Identifying genetic variants in #imprinting disorders, Beckwith–Wiedemann syndrome #BWS and #Pseudohypoparathyroidism ty…

30 May 2022

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Identifying genetic variants in #imprinting disorders, Beckwith–Wiedemann syndrome #BWS and #Pseudohypoparathyroidism type 1B, collaborating in Clinical Epigenetics @BioMedCentral article led by Drs Riccio & Cerrato @unicampania @CnrIgb @CNRsocial_ htt

30 May 2022

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