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Hear Res          2010;270: 110\u20138.","DOI":"10.1016\/j.heares.2010.08.015"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Ejiri,              H, Asano,                M,              Nakahata, N,                Suzuki, S,                Sato, A,                Nagamine,            N, et al.            Ultrasonography-based reference values for the cross-sectional area of            the thyroid gland in children and adolescents: The Fukushima Health Management            Survey. Clin Pediatr Endocrinol          2023;32: 52\u20137.","DOI":"10.1297\/cpe.2022-0057"},{"key":"11","unstructured":"11. Kusada,              N, Tsuge,                Y, Yagi,                H, Matsuda,                J, Nomura,                Y. A case of            Pendred\u2019s syndrome with Hashimoto\u2019s disease. Folia Endocrinol            Jpn          2008;84: 66\u20138 (in            Japanese)."},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Miyagawa,                M, Nishio,                SY, Usami,                S, Deafness            Gene Study Consortium. Mutation spectrum and            genotype-phenotype correlation of hearing loss patients caused by              <i>SLC26A4<\/i> mutations in the Japanese: a large cohort            study. J Hum Genet          2014;59: 262\u20138.","DOI":"10.1038\/jhg.2014.12"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Oto,              Y, Muroya,                K,              Hanakawa, J,                Asakura, Y,                Adachi,            M. The ratio of            serum free triiodothyronine to free thyroxine in children: a retrospective database            survey of healthy short individuals and patients with severe thyroid hypoplasia or            central hypothyroidism. Thyroid Res          2015;8: 10.","DOI":"10.1186\/s13044-015-0023-5"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Palos,              F,                Garc\u00eda-Rendueles,              ME,                Araujo-Vilar,              D, Obregon,                MJ, Calvo,                RM,                Cameselle-Teijeiro,              J, et al.            Pendred syndrome in two Galician families: insights into clinical            phenotypes through cellular, genetic, and molecular studies. J            Clin Endocrinol Metab          2008;93: 267\u201377.","DOI":"10.1210\/jc.2007-0539"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Kawasaki,                M, Ito,                M, Danno,                H, Kousaka,                K,              Nakamura, T,                Yoshioka,            W, et al.            The association between thyroid hormone balance and thyroid volume in            patients with Hashimoto thyroiditis. Endocr J          2019;66: 763\u20138.","DOI":"10.1507\/endocrj.EJ19-0063"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Mori,              K, Moteki,                H,              Miyagawa, M,                Nishio, SY,                Usami,            S. Social health            insurance-based simultaneous screening for 154 mutations in 19 deafness genes            efficiently identified causative mutations in Japanese hearing loss            patients. PLoS One          2016;11: e0162230.","DOI":"10.1371\/journal.pone.0162230"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Azaiez,              H, Booth,                KT,              Ephraim, SS,                Crone, B,                Black-Ziegelbein,              EA, Marini,                RJ, et al.            Genomic landscape and mutational signatures of deafness-associated            genes. Am J Hum Genet          2018;103: 484\u201397.","DOI":"10.1016\/j.ajhg.2018.08.006"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Bizhanova,                A, Kopp,                P. Genetics            and phenomics of Pendred syndrome. Mol Cell Endocrinol          2010;322: 83\u201390.","DOI":"10.1016\/j.mce.2010.03.006"},{"key":"19","unstructured":"19. Reardon,              W, Coffey,                R,                Chowdhury,              T, Grossman,                A, Jan,                H, Britton,                K, et al.            Prevalence, age of onset, and natural history of thyroid disease in            Pendred syndrome. J Med Genet          1999;36: 595\u20138."},{"key":"20","doi-asserted-by":"crossref","unstructured":"20. Lai,              CC, Chiu,                CY, Shiao,                AS, Tso,                YC, Wu,                YC, Tu,                TY, et al.            Analysis of the <i>SLC26A4<\/i> gene in patients with Pendred            syndrome in Taiwan. Metabolism          2007;56: 1279\u201384.","DOI":"10.1016\/j.metabol.2007.05.013"},{"key":"21","doi-asserted-by":"crossref","unstructured":"21. Hadj                Kacem, H,                Rebai, A,                Kaffel, N,                Masmoudi,            S, Abid,                M, Ayadi,                H. PDS is a            new susceptibility gene to autoimmune thyroid diseases: association and linkage            study. J Clin Endocrinol Metab          2003;88: 2274\u201380.","DOI":"10.1210\/jc.2002-021460"},{"key":"22","doi-asserted-by":"crossref","unstructured":"22. Belguith-Maalej,                S,              Rebuffat, SA,                Charfeddine,              I, Mnif,                M, Nadir,                RF, Abid,                M, et al.              <i>SLC26A4<\/i> expression among autoimmune thyroid            tissues. Immunobiology          2011;216: 571\u20138.","DOI":"10.1016\/j.imbio.2010.09.015"},{"key":"23","doi-asserted-by":"crossref","unstructured":"23. 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