Beckwith-Wiedemann syndrome caused by maternally-inherited mutation of an OCT-binding motif in the IGF2/H19 imprinting control region, ICR1.
type: Dataset
description: International audience
issued: 2026-05-27T04:50:24.158807
language: en
modified: 2026-05-27T04:50:24.158813
contact point: Organization
  fn: CCSD
keyword: beckwith-wiedemann-syndrome
keyword: dna-methylation
keyword: igf2h19-icr1
keyword: infoeu-reposemanticsarticle
keyword: journal-articles
keyword: sdvgenlife-sciences-q-biogenetics
landing page: 1018-4813

Beckwith-Wiedemann syndrome caused by maternally-inherited mutation of an OCT-binding motif in the IGF2/H19 imprinting control region, ICR1.
type: Distribution
format: HTML
issued: 2026-05-27T04:50:24.223647
modified: 2026-05-27T04:50:24.130095
access URL: https://hal.science/hal-00673674

test_moissonnage_selune
type: Agent