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Speiser PW, Arlt W, Auchus RJ, et al. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab 103: 4043-4088, 2018.","DOI":"10.1210\/jc.2018-01865"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Merke DP, Auchus RJ. Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. N Engl J Med 383: 1248-1261, 2020.","DOI":"10.1056\/NEJMra1909786"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Tajima T, Fujieda K, Nakae J, et al. Molecular basis of nonclassical steroid 21-hydroxylase deficiency detected by neonatal mass screening in Japan. J Clin Endocrinol Metab 82: 2350-2356, 1997.","DOI":"10.1210\/jc.82.7.2350"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Falhammar H, Torpy DJ. Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Presenting as Adrenal Incidentaloma: A Systematic Review and Meta-Analysis. 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Nagasaka S, Kubota K, Motegi T, et al. A case of silent 21-hydroxylase deficiency with persistent adrenal insufficiency after removal of an adrenal incidentaloma. Clin Endocrinol (Oxf) 44: 111-116, 1996.","DOI":"10.1046\/j.1365-2265.1996.631456.x"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Speiser PW, Dupont J, Zhu D, et al. Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Clin Invest 90: 584-595, 1992.","DOI":"10.1172\/JCI115897"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Witchel SF, Bhamidipati DK, Hoffman EP, Cohen JB. Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.. J Clin Endocrinol Metab 81: 4081-4088, 1996.","DOI":"10.1210\/jcem.81.11.8923864"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Bidet M, Bellanne-Chantelot C, Galand-Portier MB, et al. 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