Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

Human Molecular Genetics (1996) - Comments
pubmed: 8968759 issn: 0964-6906 doi: 10.1093/hmg/5.12.2027 issn: 1460-2083

K W Brown, A J Villar, W Bickmore, J Clayton-Smith, D Catchpoole, E R Maher, W Reik