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Chrousos GP, Loriaux DL, Mann DL, Cutler GB Jr. Late-onset 21-hydroxylase deficiency mimicking idiopatic hirsutism or polycysticovarian disease. Ann Intern Med 96: 143-148, 1982.","DOI":"10.7326\/0003-4819-96-2-143"},{"key":"6","unstructured":"6. Azziz R, Dewailly D, Owerbach D. 1994 Clinical review 56: Nonclassic adrenal hyperplasia: current concepts. J Clin Endocrinol Metab 78: 810-815, 1994."},{"key":"7","unstructured":"7. Brodie BL, Wentz AC. Late onset congenital adrenal hyperplasia: a gynecologist's perspective. Fertil Steril 48: 175-188, 1987."},{"key":"8","unstructured":"8. Cobin RH, Futterweit W, Fiedler RP, Thornton JC. Adrenocoticotropic hormone testing in idiopathic hirsutism and polycystic ovarian disease: a test of limited usefulness. Fertil Steril 44: 224-226, 1985."},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Benjamin F, Deutsch S, Saperstein H, Seltzer VL. Prevalence of and markers for the attenuated form of congenital adrenal hyperplasia and hyperprolactinemia masquerading as polycystic ovarian disease. Fertil Steril 46: 215-221, 1986.","DOI":"10.1016\/S0015-0282(16)49514-2"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Robyr D, Llor J, Gaudin G, Schneider N. Polycystic ovary syndrome and congenital adrenal hyperplasia: a different entity for comparable phenotypes? Rev Med Suisse 3: 1595-1596, 1598, 1600-1601, 2007.","DOI":"10.53738\/REVMED.2007.3.116.1595"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Aziz R, Rafi A, Smith BR, Bradley EL Jr, Zacur HA. On the origin of the elevated 17-hydroxy-progesterone levels after adrenal stimulation in hyperandrogenism. J Clin Endocrinol Metab 70: 431-436, 1990.","DOI":"10.1210\/jcem-70-2-431"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Sahin Y, Kelestimur F. The frequency of late-onset 21-hydroxylase and 11 beta-hydroxylase deficiency in women with polycystic ovary syndrome. Eur J Endocrinol 137: 670-674, 1997.","DOI":"10.1530\/eje.0.1370670"},{"key":"13","unstructured":"13. Avivi I, Pollack S, Gideoni O, Linn S, Blumenfeld Z. Overdiagnosis of 21-hydroxylase late onset congenital adrenal hyperplasia: correlation of corticotropin test and human leukocyte antigen typing. Fertil Steril 66: 557-563, 1996."},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Yarman S, Dursun A, Oguz F, Alagol F. 2004 The prevalence, molecular analysis and HLA typing of late-onset 21-hydroxylase deficiency in Turkish woman with hirsutism and polycystic ovary. Endocr J 51: 31-36, 2004.","DOI":"10.1507\/endocrj.51.31"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Unluhizarci K, Kula M, Dundar M. The prevalence of non-classic adrenal hyperplasia among Turkish women with hyperandrogenism. 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Cyclic Cushing syndrome: definitions and treatment implications. Neurosurg Focus 23: E4; discussion E4a, 2007."},{"key":"20","unstructured":"20. Ragnarsson O, Johannsson G. Management of endocrine disease: Cushing's syndrome: a structured short- and long-term management plan for patients in remission. Eur J Endocrinol 169: R139-R152, 2013."},{"key":"21","doi-asserted-by":"crossref","unstructured":"21. Gupta P, Goyal S, Gonzalez-Mendoza LE, et al. Corticotropin-independent cushing syndrome in a child with an ovarian tumor misdiagnosed as nonclassic congenital adrenal hyperplasia. Endocr Pract 14: 875-879, 2008.","DOI":"10.4158\/EP.14.7.875"},{"key":"22","doi-asserted-by":"crossref","unstructured":"22. Campos SP, MacGillivray MH. Preclinical Cushing syndrome due to an adrenocortical adenoma mimicking late-onset congenital adrenal hyperplasia. Clin Pediatr 33: 246-248, 1994.","DOI":"10.1177\/000992289403300412"},{"key":"23","unstructured":"23. Loh V, Krishnan B, Prentice M, Panahloo A, Seal L. Late onset congenital adrenal hyperplasia masquerading as subclinical Cushing's syndrome. Endocrine Abstracts 19: 72, 2009."},{"key":"24","doi-asserted-by":"crossref","unstructured":"24. Dall'Asta C, Barbetta L, Libé R, Passini E, Ambrosi B. Coexistence of 21-hydroxylase and 11 beta-hydroxylase deficiency in adrenal incidentalomas and in subclinical Cushing's syndrome. Horm Res 57: 192-196, 2002.","DOI":"10.1159\/000058381"},{"key":"25","doi-asserted-by":"crossref","unstructured":"25. Boronat M, Carrillo A, Ojeda A, et al. Clinical manifestations and hormonal profile of two women with Cushing's disease and mild deficiency of 21-hydroxylase. J Endocrinol Invest 27: 583-590, 2004.","DOI":"10.1007\/BF03347484"},{"key":"26","doi-asserted-by":"crossref","unstructured":"26. O'Bryan RM, Smith RW Jr, Fine G, Mllinger RC. Congenital adrenocortical hyperplasia with Cushing's syndrome. 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