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Ford, G, LaFranchi, SH. Screening for congenital hypothyroidism: a worldwide view of strategies. Best Pract Res Clin Endocrinol Metab 2014;28: 175\u201387.","DOI":"10.1016\/j.beem.2013.05.008"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. van Trotsenburg, P, Stoupa, A, L\u00e9ger, J, Rohrer, T, Peters, C, Fugazzola, L, et al. Congenital hypothyroidism: A 2020-2021 consensus guidelines update-an ENDO-European reference network initiative endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology. Thyroid 2021;31: 387\u2013419.","DOI":"10.1089\/thy.2020.0333"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Di Palma, T, Nitsch, R, Mascia, A, Nitsch, L, Di Lauro, R, Zannini, M. The paired domain-containing factor Pax8 and the homeodomain-containing factor TTF-1 directly interact and synergistically activate transcription. 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Iwahashi-Odano, M, Nagasaki, K, Fukami, M, Nishioka, J, Yatsuga, S, Asakura, Y, et al. Congenital hypothyroidism due to truncating PAX8 mutations: a case series and molecular function studies. J Clin Endocrinol Metab 2020;105: 105.","DOI":"10.1210\/clinem\/dgaa584"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Al Taji, E, Biebermann, H, L\u00edmanov\u00e1, Z, Hn\u00edkov\u00e1, O, Zikmund, J, Dame, C, et al. Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism. Eur J Endocrinol 2007;156: 521\u20139.","DOI":"10.1530\/EJE-06-0709"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Carvalho, A, Hermanns, P, Rodrigues, AL, Sousa, I, Anselmo, J, Bikker, H, et al. 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Meeus, L, Gilbert, B, Rydlewski, C, Parma, J, Roussie, AL, Abramowicz, M, et al. Characterization of a novel loss of function mutation of PAX8 in a familial case of congenital hypothyroidism with in-place, normal-sized thyroid. J Clin Endocrinol Metab 2004;89: 4285\u201391.","DOI":"10.1210\/jc.2004-0166"},{"key":"25","doi-asserted-by":"crossref","unstructured":"25. Narumi, S, Araki, S, Hori, N, Muroya, K, Yamamoto, Y, Asakura, Y, et al. Functional characterization of four novel PAX8 mutations causing congenital hypothyroidism: new evidence for haploinsufficiency as a disease mechanism. Eur J Endocrinol 2012;167: 625\u201332.","DOI":"10.1530\/EJE-12-0410"},{"key":"26","doi-asserted-by":"crossref","unstructured":"26. Iwahashi-Odano, M, Fujisawa, Y, Ogata, T, Nakashima, S, Muramatsu, M, Narumi, S. Identification and functional characterization of a novel <i>PAX8<\/i> mutation (p.His39Pro) causing familial thyroid hypoplasia. 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Tanaka, T, Yokoya, S, Kato, N, Ito, Y, Tachibana, K, Sugihara, S, et al. Basic approach to the evaluation of height and weight in Japanese children. J Jpn Ass Hum Auxo 2011;17: 84\u201399 (in Japanese)."},{"key":"40","doi-asserted-by":"crossref","unstructured":"40. Delvecchio, M, Salerno, M, Vigone, MC, Wasniewska, M, Popolo, PP, Lapolla, R, et al. Levothyroxine requirement in congenital hypothyroidism: a 12-year longitudinal study. 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