Imprinting Mutation in the Beckwith-Wiedemann Syndrome Leads to Biallelic IGF2 expression through an H19 -Independent Pathway

Author: Brown Keith W.   Villar Angela J.   Bickmore Wendy   Clayton-Smith Jill   Catchpoole Daniel   Maher Eamonn R.   Reik Wolf  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.5, Iss.12, 1996-12, pp. : 2027-2032

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