Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Reference59 articles.
1. Ahlgren R, Yanase T, Simpson ER, Winter JS, Waterman MR (1992) Compound heterozygous mutations (Arg 239»stop, Pro 342»Thr) in the CYP17 (P450 17 alpha) gene lead to ambiguous external genitalia in a male patient with partial combined 17 alpha-hydroxylase 17,20-lyase deficiency. J Clin Endocrinol Metab 74:667–672
2. Akesode FA, Meyer WJ III, Migeon CJ (1977) Male pseudohermaphroditism with gynaecomastia due to testicular 17-ketosteroid reductase deficiency. Clin Endocrinol (Oxf) 7:443–452
3. Andersson S, Berman DM, Jenkins EP, Russell DW (1991) Deletion of steroid 5alpha-reductase 2 gene in male pseudohermaphroditism. Nature 354:159–161
4. Balducci R, Toscano V, Wright F, Bozzolan F, Di Piero G, Maroder M, Panei P, Sciarra F, Boscherini B (1985) Familial male pseudohermaphroditism with gynaecomastia due to 17β-hydroxysteroid dehydrogenase deficiency. A report of 3 cases. Clin Endocrinol (Oxf) 23:439–444
5. Biglieri EG, Herron MA, Brust N (1966) 17-Hydroxylase deficiency in man. J Clin Invest 45:1946–1954
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献