Literature DB >> 18957982

Wilms tumor and constitutional epigenetic defects.

Andrea Riccio.   

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Year:  2008        PMID： 18957982     DOI： 10.1038/ng1108-1272

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  1 in total

1.  A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome.

Authors:  Agostina De Crescenzo; Filomena Coppola; Pietro Falco; Italo Bernardo; Gaetano Ausanio; Flavia Cerrato; Luigi Falco; Andrea Riccio
Journal:  Eur J Med Genet       Date:  2011-05-04       Impact factor: 2.708
  1 in total

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