Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (sporPHP1B).

Serum FGF-21 levels are associated with worsened radial trabecular bone microarchitecture...Hypoparathyroidism – disease update and emerging treatments.