SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Miho Ishida, New developments in Silver–Russell syndrome and implications for clinical practice, Epigenomics, 2016, 8, 4, 563

    CrossRef

  2. 2
    Doreen Heckmann, Christina Urban, Karin Weber, Kai Kannenberg, Gerhard Binder, Decreased expression of cell proliferation-related genes in clonally derived skin fibroblasts from children with Silver-Russell syndrome is independent of the degree of 11p15 ICR1 hypomethylation, Clinical Epigenetics, 2015, 7, 1, 5

    CrossRef

  3. 3
    A. R. Prickett, M. Ishida, S. Böhm, J. M. Frost, W. Puszyk, S. Abu-Amero, P. Stanier, R. Schulz, G. E. Moore, R. J. Oakey, Genome-wide methylation analysis in Silver–Russell syndrome patients, Human Genetics, 2015, 134, 3, 317

    CrossRef

  4. 4
    Salah Azzi, Walid Abi Habib, Irene Netchine, Beckwith–Wiedemann and Russell–Silver Syndromes, Current Opinion in Endocrinology & Diabetes and Obesity, 2014, 21, 1, 30

    CrossRef

  5. 5
    Salah Azzi, Annick Blaise, Virginie Steunou, Madeleine D. Harbison, Jennifer Salem, Frédéric Brioude, Sylvie Rossignol, Walid Abi Habib, Nathalie Thibaud, Cristina Das Neves, Marilyne Le Jule, Cécile Brachet, Claudine Heinrichs, Yves Le Bouc, Irène Netchine, Complex Tissue-Specific Epigenotypes in Russell–Silver Syndrome Associated with 11p15 ICR1 Hypomethylation, Human Mutation, 2014, 35, 10
  6. 6
    Katariina Hannula-Jouppi, Mari Muurinen, Marita Lipsanen-Nyman, Lovisa E Reinius, Sini Ezer, Dario Greco, Juha Kere, Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7, Epigenetics, 2014, 9, 3, 351

    CrossRef

  7. 7
    Carolina Isabel Galaz-Montoya, Constanza García-Delgado, Alicia Cervantes-Peredo, Leticia García-Morales, Verónica Fabiola Morán-Barroso, Perfil clínico de una cohorte de pacientes con síndrome de Silver-Russell atendidos en el Hospital Infantil de México Federico Gómez de 1998 a 2012, Boletín Médico del Hospital Infantil de México, 2014, 71, 4, 218

    CrossRef

  8. 8
    Stéphanie Maupetit-Méhouas, Salah Azzi, Virginie Steunou, Nathalie Sakakini, Caroline Silve, Christelle Reynes, Guiomar Perez de Nanclares, Boris Keren, Sandra Chantot, Anne Barlier, Agnès Linglart, Irène Netchine, Simultaneous Hyper- and Hypomethylation at Imprinted Loci in a Subset of Patients with GNAS Epimutations Underlies a Complex and Different Mechanism of Multilocus Methylation Defect in Pseudohypoparathyroidism Type 1b, Human Mutation, 2013, 34, 8
  9. 9
    Miho Ishida, Gudrun E. Moore, The role of imprinted genes in humans, Molecular Aspects of Medicine, 2013, 34, 4, 826

    CrossRef

  10. 10
    Kai Kannenberg, Karin Weber, Cathrin Binder, Christina Urban, Hans-Joachim Kirschner, Gerhard Binder, IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome, Clinical Epigenetics, 2012, 4, 1, 15

    CrossRef