Mechanisms causing imprinting defects in familial BeckwithWiedemann syndrome with Wilms' tumour

By Sparago Angela   Russo Silvia   Cerrato Flavia   Ferraiuolo Serena   Castorina Pierangela   Selicorni Angelo   Schwienbacher Christine   Negrini Massimo   Ferrero Giovanni Battista   Silengo Margherita Cirillo   Anichini Cecilia   Larizza Lidia   Riccio Andrea  

Human Molecular Genetics, Vol. 16, Iss. 3, 2007-02 ,pp. : 254-264

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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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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An association between variants in the IGF2 gene and Beckwith–Wiedemann syndrome: interaction between genotype and epigenotype

By Murrell Adele  

Human Molecular Genetics, Vol. 13, Iss. 2, 2004-01 ,pp. : 247-255

Oxford University Press

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