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Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome

  • Published:2011-01-31 Issue:7 Volume:20 Page:1363-1374
  • ISSN:1460-2083
  • Container-title:Human Molecular Genetics
  • language:en
  • Short-container-title:

Author:

Nativio Raffaella,Sparago Angela,Ito Yoko,Weksberg Rosanna,Riccio Andrea,Murrell Adele

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Reference34 articles.

1. Beckwith-Wiedemann syndrome;Weksberg;Eur. J. Hum. Genet.,2010

2. Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures;Eggermann;Horm. Res.,2009

3. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene;Bell;Nature,2000

4. CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus;Hark;Nature,2000

5. Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function;Szabo;Curr. Biol.,2000
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