Similar articles

• Two types of male pseudohermaphroditism due to 17, 20-desmolase deficiency.

  Zachmann M, Werder EA, Prader A. Zachmann M, et al. J Clin Endocrinol Metab. 1982 Sep;55(3):487-90. doi: 10.1210/jcem-55-3-487. J Clin Endocrinol Metab. 1982. PMID: 6212590
• In vitro fertilization as a diagnostic and therapeutic tool in a patient with partial 17,20-desmolase deficiency.

  Pellicer A, Miró F, Sampaio M, Gómez E, Bonilla-Musoles FM. Pellicer A, et al. Fertil Steril. 1991 May;55(5):970-5. doi: 10.1016/s0015-0282(16)54308-8. Fertil Steril. 1991. PMID: 1902422
• Familial male pseudohermaphroditism due to 17-20-desmolase deficiency. I. In vivo endocrine studies.

  Forest MG, Lecornu M, de Peretti E. Forest MG, et al. J Clin Endocrinol Metab. 1980 May;50(5):826-33. doi: 10.1210/jcem-50-5-826. J Clin Endocrinol Metab. 1980. PMID: 6246133
• 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.
• [17,20-Desmolase deficiency].

  Yanase T, Nawata H. Yanase T, et al. Ryoikibetsu Shokogun Shirizu. 1993;(1):911-4. Ryoikibetsu Shokogun Shirizu. 1993. PMID: 7757785 Review. Japanese. No abstract available.