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 378Â kb)
2018-02-06 05:00:00
GNAS
Imprinting
Mosaicism
Pseudohypoparathyroidism
Albright hereditary osteodystrophy
PTH resistance
Epigenetics
Methylation defects