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This page is a summary of: Simultaneous Hyper- and Hypomethylation at Imprinted Loci in a Subset of Patients withGNASEpimutations Underlies a Complex and Different Mechanism of Multilocus Methylation Defect in Pseudohypoparathyroidism Type 1b, Human Mutation, May 2013, Wiley,
DOI: 10.1002/humu.22352.
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