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

Brown Keith (686858)

Publication date

January 2015

DOI

10.6084/m9.figshare.1296134.v2

Abstract

<p>Original data used to make figure 2A and 2B compared to the published data for our paper puiblsihed in:<br>Human Molecular Genetics (1996) 12, 2027-2032 </p

Extracted data

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

Abstract

Extracted data

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

Abstract

Extracted data

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