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Journal Abstract Search

367 related items for PubMed ID: 26691664

  • 1. First report on concordant monozygotic twins with Silver-Russell syndrome and ICR1 hypomethylation.
    Riess A, Binder G, Ziegler J, Begemann M, Soellner L, Eggermann T.
    Eur J Med Genet; 2016 Jan; 59(1):1-4. PubMed ID: 26691664
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  • 2. 11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome.
    Abi Habib W, Brioude F, Azzi S, Salem J, Das Neves C, Personnier C, Chantot-Bastaraud S, Keren B, Le Bouc Y, Harbison MD, Netchine I.
    Hum Mutat; 2017 Jan; 38(1):105-111. PubMed ID: 27701793
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  • 3. Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome.
    Azzi S, Steunou V, Tost J, Rossignol S, Thibaud N, Das Neves C, Le Jule M, Habib WA, Blaise A, Koudou Y, Busato F, Le Bouc Y, Netchine I.
    J Med Genet; 2015 Jan; 52(1):53-60. PubMed ID: 25395389
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  • 4. Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilization.
    Cocchi G, Marsico C, Cosentino A, Spadoni C, Rocca A, De Crescenzo A, Riccio A.
    Am J Med Genet A; 2013 Oct; 161A(10):2652-5. PubMed ID: 24038823
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  • 5. Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues.
    Begemann M, Spengler S, Kanber D, Haake A, Baudis M, Leisten I, Binder G, Markus S, Rupprecht T, Segerer H, Fricke-Otto S, Mühlenberg R, Siebert R, Buiting K, Eggermann T.
    Clin Genet; 2011 Jul; 80(1):83-8. PubMed ID: 20738330
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  • 6. A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family.
    Jurkiewicz D, Kugaudo M, Skórka A, Śmigiel R, Smyk M, Ciara E, Chrzanowska K, Krajewska-Walasek M.
    Am J Med Genet A; 2017 Jan; 173(1):72-78. PubMed ID: 27612309
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  • 7. Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome?
    Sparago A, Cerrato F, Riccio A.
    Clin Epigenetics; 2018 Jan; 10():23. PubMed ID: 29484033
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  • 14. Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver-Russell syndrome.
    Kannenberg K, Urban C, Binder G.
    Clin Genet; 2012 Apr; 81(4):366-77. PubMed ID: 22248018
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  • 15. Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients.
    Rovina D, La Vecchia M, Cortesi A, Fontana L, Pesant M, Maitz S, Tabano S, Bodega B, Miozzo M, Sirchia SM.
    Sci Rep; 2020 May 19; 10(1):8275. PubMed ID: 32427849
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  • 17. Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype.
    Kagami M, Mizuno S, Matsubara K, Nakabayashi K, Sano S, Fuke T, Fukami M, Ogata T.
    Eur J Hum Genet; 2015 Aug 19; 23(8):1062-7. PubMed ID: 25351781
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  • 18. Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders.
    Demars J, Shmela ME, Rossignol S, Okabe J, Netchine I, Azzi S, Cabrol S, Le Caignec C, David A, Le Bouc Y, El-Osta A, Gicquel C.
    Hum Mol Genet; 2010 Mar 01; 19(5):803-14. PubMed ID: 20007505
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