Testicular in vitro conversion of progesterone to testosterone and androstenedione in 17α-hydroxylase deficiency
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry
Reference16 articles.
1. 17-hydroxylation deficiency in man;Biglieri;J. clin. Invest.,1966
2. Male pseudohermaphroditism with hypertension due to a 17α-hydroxylation deficiency;Tourniare;Clin. Endocr., Oxf.,1976
3. 17α-hydroxylase deficiency of the gonads and adrenals in a male pseudohermaphrodite;Hammerstein;Acta Endocr., Copenh. Suppl.,1973
4. Partial hypopituitarism following septic peritonitis with shock;Arafah;Arch. Intern. Med.,1978
5. Dehydroepiandrosterone sulfate in plasma: Hydrolysis, extraction and radioimmunoassay;Metcalf;Steroids,1976
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1. Familial partial 17,20-desmolase and 17 alpha-hydroxylase deficiency presenting as infertility;Journal of Assisted Reproduction and Genetics;2003
2. Disposition of lupanine and 13-hydroxylupanine in man;Xenobiotica;1994-01
3. Steroid enzyme defects leading to male pseudohermaphroditism;The Indian Journal of Pediatrics;1992-07
4. 17α-Hydroxylase/17,20-Lyase Deficiency: From Clinical Investigation to Molecular Definition*;Endocrine Reviews;1991-02
5. A Case of Male Pseudohermaphroditism due to 17α-Hydroxylase Deficiency and Hormonal Profiles in the Nuclear Family*;The Journal of Clinical Endocrinology & Metabolism;1990-08
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