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Weinstein,                LS, Yu,                S, Warner,                DR, Liu,                J. Endocrine            manifestations of stimulatory G protein alpha-subunit mutations and the role of genomic            imprinting. Endocr Rev          2001;22: 675\u2013705.","DOI":"10.1210\/edrv.22.5.0439"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Yu,                S, Yu,                D, Lee,                E, Eckhaus,                M, Lee,                R, Corria,                Z, et al.            Variable and tissue-specific hormone resistance in heterotrimeric Gs            protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of            the gsalpha gene. Proc Natl Acad Sci USA          1998;95: 8715\u201320.","DOI":"10.1073\/pnas.95.15.8715"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. 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Pseudohypoparathyroidism and Gs\u03b1-cAMP-linked disorders: current view and            open issues. Nat Rev Endocrinol          2016;12: 347\u201356.","DOI":"10.1038\/nrendo.2016.52"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Kuzmiak,                HA, Maquat,                LE. Applying            nonsense-mediated mRNA decay research to the clinic: progress and            challenges. Trends Mol Med          2006;12: 306\u201316.","DOI":"10.1016\/j.molmed.2006.05.005"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Richards,                S, Aziz,                N, Bale,                S, Bick,                D, Das,                S,                Gastier-Foster,              J, et al.            ACMG Laboratory Quality Assurance Committee.            Standards and guidelines for the interpretation of sequence variants: a            joint consensus recommendation of the American College of Medical Genetics and Genomics            and the Association for Molecular Pathology. Genet Med          2015;17: 405\u201324.","DOI":"10.1038\/gim.2015.30"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Sano,              S, Nakamura,                A,                Matsubara,              K, Nagasaki,                K, Fukami,                M, Kagami,                M, et al.            (Epi)genotype-phenotype analysis in 69 Japanese patients with            pseudohypoparathyroidism type I. J Endocr Soc          2017;2: 9\u201323.","DOI":"10.1210\/js.2017-00293"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Pinsker,                JE, Rogers,                W, McLean,                S,              Schaefer, FV,                Fenton,            C.            Pseudohypoparathyroidism type 1a with congenital            hypothyroidism. J Pediatr Endocrinol Metab          2006;19: 1049\u201352.","DOI":"10.1515\/JPEM.2006.19.8.1049"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Shoemaker,                AH,              J\u00fcppner,            H. Nonclassic            features of pseudohypoparathyroidism type 1A. Curr Opin            Endocrinol Diabetes Obes          2017;24: 33\u20138.","DOI":"10.1097\/MED.0000000000000306"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Thiele,              S, Werner,                R,                Gr\u00f6tzinger,              J, Brix,                B, Staedt,                P, Struve,                D, et al.            A positive genotype-phenotype correlation in a large cohort of patients            with pseudohypoparathyroidism type Ia and pseudo-pseudohypoparathyroidism and 33 newly            identified mutations in the GNAS gene. 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