Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith–Wiedemann syndrome region in chromosome 11p15.5

By Davies K.E.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1149-1159

Oxford University Press

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

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

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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

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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

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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

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