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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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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Imprinting of IGF2 and H19 : Lack of Reciprocity in Sporadic Beckwith-Wiedemann Syndrome

By Joyce Johanna A.   Lam Wayne K.  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1543-1548

Oxford University Press

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Imprinting Mutation in the Beckwith-Wiedemann Syndrome Leads to Biallelic IGF2 expression through an H19 -Independent Pathway

By Brown Keith W.   Villar Angela J.   Bickmore Wendy   Clayton-Smith Jill   Catchpoole Daniel   Maher Eamonn R.   Reik Wolf  

Human Molecular Genetics, Vol. 5, Iss. 12, 1996-12 ,pp. : 2027-2032

Oxford University Press

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The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine BeckwithWiedemann region

By Lefebvre Louis   Mar Lynn   Bogutz Aaron   Oh-McGinnis Rosemary   Mandegar Mohammad A.   Paderova Jana   Gertsenstein Marina   Squire Jeremy A.   Nagy Andras  

Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4255-4267

Oxford University Press

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