Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann Syndrome

Publisher： Karger

E-ISSN： 1661-8777|5|1|41-46

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.5, Iss.1, 2013-11, pp. : 41-46

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

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

A Microdeletion at 12q24.31 Can Mimic Beckwith-Wiedemann Syndrome Neonatally

By  

Molecular Syndromology, Vol. 1, Iss. 1, 2010-01 ,pp. : 42-45

Karger

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology

By  

Molecular Syndromology, Vol. 7, Iss. 3, 2016-07 ,pp. : 110-121

Karger

Access to resources Recommend Favorite