Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour-Reference-Cited by-同舟云学术

Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour

Published:2006-12-11 Issue:3 Volume:16 Page:254-264
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

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

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/16/3/254/1679261/ddl448.pdf

Reference49 articles.

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2. Genomic imprinting: intricacies of epigenetic regulation in clusters;Verona;Annu. Rev. Cell Dev. Biol.,2003

3. A census of mammalian imprinting;Morison;Trends Genet.,2005

4. Epigenetic deregulation of genomic imprinting in human disorders and following assisted reproduction;Arnaud;Birth Defects Res. C Embryo Today,2005

5. Beckwith–Wiedemann syndrome: imprinting in clusters revisited;Maher;J. Clin. Invest.,2000

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