Different mechanisms cause imprinting defects at the IGF2 / H19 locus in BeckwithWiedemann syndrome and Wilms' tumour

By Cerrato Flavia   Sparago Angela   Verde Gaetano   De Crescenzo Agostina   Citro Valentina   Cubellis Maria Vittoria   Rinaldi Maria Michela   Boccuto Luigi   Neri Giovanni   Magnani Cinzia   D'Angelo Paolo   Collini Paola   Perotti Daniela   Sebastio Gianfranco   Maher Eamonn R.   Riccio Andrea  

Human Molecular Genetics, Vol. 17, Iss. 10, 2008-05 ,pp. : 1427-1435

Oxford University Press

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

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

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1363-1374

Oxford University Press

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Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA

By Cerrato Flavia  

Human Molecular Genetics, Vol. 12, Iss. 23, 2003-12 ,pp. : 3123-3132

Oxford University Press

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Heritable rather than age-related environmental and stochastic factors dominate variation in DNA methylation of the human IGF2/H19 locus

By Heijmans Bastiaan T.   Kremer Dennis   Tobi Elmar W.   Boomsma Dorret I.   Slagboom P. Eline  

Human Molecular Genetics, Vol. 16, Iss. 5, 2007-03 ,pp. : 547-554

Oxford University Press

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CTCF binding sites promote transcription initiation and prevent DNA methylation on the maternal allele at the imprinted H19/Igf2 locus

By Engel Nora   Thorvaldsen Joanne L.   Bartolomei Marisa S.  

Human Molecular Genetics, Vol. 15, Iss. 19, 2006-10 ,pp. : 2945-2954

Oxford University Press

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