(Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1BTatsuki Urakawa, Masayo Kagami, Maki Fukami et al.|European Journal of Endocrinology|2023Cited by 4
Epigenotype-phenotype analysis in 84 patients with pseudohypoparathyroidism type 1B based on the methylation patterns of four differentially methylated regions on the GNAS locusTatsuki Urakawa, Masayo Kagami, Sayaka Kawashima et al.|Figshare|2023Cited by 0
Molecular and clinical studies in 84 patients with pseudohypoparathyroidism type 1BTatsuki Urakawa, Masayo Kagami, Sayaka Kawashima et al.|Figshare|2023Cited by 0
Epigenotype-phenotype analysis in 84 patients with pseudohypoparathyroidism type 1B based on the methylation patterns of four differentially methylated regions on the GNAS locusTatsuki Urakawa, Masayo Kagami, Sayaka Kawashima et al.|Figshare|2023Cited by 0
Severe infantile obesity with a maternal <i>GNAS</i> deletion and multi-locus imprinting disturbance including hypomethylation of the <i>KCNQ1OT1</i>:TSS-DMRTatsuki Urakawa, Masayo Kagami, Masaharu Shimada et al.|Clinical Pediatric Endocrinology|2026Cited by 0