Additional file 1: Figure S1. of Mosaicism for GNAS methylation defects associated with pseudohypoparathyroidism type 1B arose in early post-zygotic phases Francesca Elli Paolo Bordogna Maura Arosio Anna Spada Giovanna Mantovani 10.6084/m9.figshare.5862633.v1 https://springernature.figshare.com/articles/journal_contribution/Additional_file_1_Figure_S1_of_Mosaicism_for_GNAS_methylation_defects_associated_with_pseudohypoparathyroidism_type_1B_arose_in_early_post-zygotic_phases/5862633 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 378 kb) 2018-02-06 05:00:00 GNAS Imprinting Mosaicism Pseudohypoparathyroidism Albright hereditary osteodystrophy PTH resistance Epigenetics Methylation defects