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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Tumor development in the Beckwith–Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1

By Weksberg Rosanna  

Human Molecular Genetics, Vol. 10, Iss. 26, 2001-12 ,pp. : 2989-3000

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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Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith–Wiedemann syndrome

By Olney A.  

Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1317-1325

Oxford University Press

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Sequence conservation and variability of imprinting in the Beckwith–Wiedemann syndrome gene cluster in human and mouse

By Paulsen Martina  

Human Molecular Genetics, Vol. 9, Iss. 12, 2000-07 ,pp. : 1829-1841

Oxford University Press

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