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

Author： Weksberg Rosanna  

Publisher： Oxford University Press

ISSN： 1460-2083

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

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

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

Access to resources Recommend Favorite

The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases

By Chiesa Nicoletta   De Crescenzo Agostina   Mishra Kankadeb   Perone Lucia   Carella Massimo   Palumbo Orazio   Mussa Alessandro   Sparago Angela   Cerrato Flavia   Russo Silvia   Lapi Elisabetta   Cubellis Maria Vittoria   Kanduri Chandrasekhar   Cirillo Silengo Margherita   Riccio Andrea   Ferrero Giovanni Battista  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 10-25

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Oxford University Press

Access to resources Recommend Favorite