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Paper Details

A genome-wide screen in human embryonic stem cells reveals novel sites of allele-specific histone modification associated with known disease loci.
Epigenetics Chromatin
12
2012
ASE, ASHM, Human, allele, allele-specific expression, chromosome copies, developmental syndromes, disease loci, embryonic stem cells, hESCs, histone, human, human embryonic stem cells, imprinted regions, risk loci
Author NameAffiliation
James G D PrendergastMRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital
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