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(2022) 17\u03b1-hydroxylase\/17,20-lyase deficiency in 46,XY: our experience and review of literature. J Endocr Soc 6: bvac011.","DOI":"10.1210\/jendso\/bvac011"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2 New MI (1970) Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency. J Clin Invest 49: 1930\u20131941.","DOI":"10.1172\/JCI106412"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3 Kagimoto M, Winter JS, Kagimoto K, Simpson ER, Waterman MR (1988) Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: molecular basis of one example of combined 17 alpha-hydroxylase\/17,20 lyase deficiency. Mol Endocrinol 2: 564\u2013570.","DOI":"10.1210\/mend-2-6-564"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4 Biglieri EG, Herron MA, Brust N (1966) 17-hydroxylation deficiency in man. 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Horm Metab Res 24: 339\u2013341.","DOI":"10.1055\/s-2007-1003328"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8 Moreira AC, Leal AM, Castro M (1990) Characterization of adrenocorticotropin secretion in a patient with 17 alpha-hydroxylase deficiency. J Clin Endocrinol Metab 71: 86\u201391.","DOI":"10.1210\/jcem-71-1-86"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9 Zhang Y, Zhang X, Wang Y, Hua K, Ding J (2018) Genetic defect of a combined 17 \u03b1-hydroxylase\/17,20-lyase deficiency patient with adrenal crisis. Gynecol Endocrinol 34: 540\u2013544.","DOI":"10.1080\/09513590.2017.1417981"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10 Hinz L, Pacaud D, Kline G (2018) Congenital adrenal hyperplasia causing hypertension: an illustrative review. 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