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Asian J            Androl          2017;19: 168\u201372."},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Vorona,              E, Zitzmann,                M, Gromoll,                J,              Sch\u00fcring, AN,                Nieschlag,              E. Clinical,            endocrinological, and epigenetic features of the 46,XX male syndrome, compared with            47,XXY Klinefelter patients. J Clin Endocrinol Metab          2007;92: 3458\u201365.","DOI":"10.1210\/jc.2007-0447"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Chen,              T, Tian,                L, Wu,                F, Xuan,                X, Ma,                G, Tang,                R, et al.            Clinical and genetic analysis in males with 46,XX disorders of sex            development: A reproductive centre experience of 144 cases.            Andrologia          2019;51: e13232.","DOI":"10.1111\/and.13232"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Hamada,              AJ, Esteves,                SC,              Agarwal,            A. A            comprehensive review of genetics and genetic testing in azoospermia.            Clinics (Sao Paulo)          2013;68(Suppl 1):            39\u201360.","DOI":"10.6061\/clinics\/2013(Sup01)06"},{"key":"7","unstructured":"7. Manuel,              M, Katayama,                PK, Jones,              Jr,            HW. Am J Obstet            Gynecol          1976;124: 293\u2013300."},{"key":"8","unstructured":"8. Guerreo-Fdez,                J, Bonis,                AB. Endocrinologia          pedi\u00e1trica, chapter 86. In: Manual de Diagn\u00f3stico y Terap\u00e9utica em            Pediatr\u00eda<i>.<\/i> 6<sup>th<\/sup> edition. 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