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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The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster

By Cerrato Flavia  

Human Molecular Genetics, Vol. 14, Iss. 4, 2005-02 ,pp. : 503-511

Oxford University Press

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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

Oxford University Press

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Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith–Wiedemann syndrome

By Horike Shin-ichi   Mitsuya Kohzoh   Meguro Makiko   Kotobuki Noriko   Kashiwagi Akiko   Notsu Tomomi   Schulz ThomasC.   Shirayoshi Yasuaki   Oshimura Mitsuo  

Human Molecular Genetics, Vol. 9, Iss. 14, 2000-09 ,pp. : 2075-2083

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Distant cis -elements regulate imprinted expression of the mouse p57 Kip2 ( Cdkn1c ) gene: implications for the human disorder, Beckwith–Wiedemann syndrome

By John R.M.   Ainscough J.F.   Barton S.C.   Surani M.A.  

Human Molecular Genetics, Vol. 10, Iss. 15, 2001-07 ,pp. : 1601-1609

Oxford University Press

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