Additional file 1: Figure S1. of Mosaicism for GNAS methylation defects associated with pseudohypoparathyroidism type 1B arose in early post-zygotic phases
journal contributionposted on 06.02.2018 by Francesca Elli, Paolo Bordogna, Maura Arosio, Anna Spada, Giovanna Mantovani
Any type of content formally published in an academic journal, usually following a peer-review process.
Methylation-specific probes location, GR37/hg19. Table S1. Raw methylation ratios. Table S2. Variable number tandem repeats (VNTRs) in the 20q region analysed to exclude uniparental disomy (UPD). (DOCX 378Â kb)