Similar articles

• [A case of male pseudohermaphroditism due to 17,20-desmolase deficiency].

  Nomura H, Yamamoto T, Kozuka Y, Taniguchi H, Toyoda N, Yamawaki T, Naka A, Nishiyama M, Sugiyama Y. Nomura H, et al. Nihon Sanka Fujinka Gakkai Zasshi. 1988 Feb;40(2):259-62. Nihon Sanka Fujinka Gakkai Zasshi. 1988. PMID: 3361182 Japanese. No abstract available.
• Prismatic cases: 17,20-desmolase (17,20-lyase) deficiency.

  Zachmann M. Zachmann M. J Clin Endocrinol Metab. 1996 Feb;81(2):457-9. doi: 10.1210/jcem.81.2.8636249. J Clin Endocrinol Metab. 1996. PMID: 8636249 No abstract available.
• Conversion from pure 17,20-desmolase- to combined 17,20-desmolase/17 alpha-hydroxylase deficiency with age.

  Zachmann M, Kempken B, Manella B, Navarro E. Zachmann M, et al. Acta Endocrinol (Copenh). 1992 Aug;127(2):97-9. doi: 10.1530/acta.0.1270097. Acta Endocrinol (Copenh). 1992. PMID: 1529667
• 17 alpha-hydroxylase/17,20-lyase deficiency: from clinical investigation to molecular definition.

  Yanase T, Simpson ER, Waterman MR. Yanase T, et al. Endocr Rev. 1991 Feb;12(1):91-108. doi: 10.1210/edrv-12-1-91. Endocr Rev. 1991. PMID: 2026124 Review. No abstract available.
• Endocrine findings in male pseudohermaphroditism.

  Zachmann M. Zachmann M. Eur J Pediatr. 1993;152 Suppl 2:S58-61. doi: 10.1007/BF02125441. Eur J Pediatr. 1993. PMID: 8339744 Review.