Elli, Francesca Bordogna, Paolo Arosio, Maura Spada, Anna Mantovani, Giovanna Additional file 1: Figure S1. of Mosaicism for GNAS methylation defects associated with pseudohypoparathyroidism type 1B arose in early post-zygotic phases 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) GNAS;Imprinting;Mosaicism;Pseudohypoparathyroidism;Albright hereditary osteodystrophy;PTH resistance;Epigenetics;Methylation defects 2018-02-06
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