共 50 条
- [32] A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (01): : 291 - 295
- [35] EFFECT OF ACTH ADMINISTRATION ON ALDOSTERONE PRODUCTION IN NON SALT-LOSING CONGENITAL ADRENAL-HYPERPLASIA JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1972, 35 (04): : 595 - +
- [36] ADRENAL 3BETA-HYDROXYSTEROID DEHYDROGENASE ACTIVITY IN NORMAL AND HYPOPHYSECTOMIZED CHICK EMBRYOS ANATOMICAL RECORD, 1970, 166 (02): : 303 - &
- [38] Two Novel Homozygous Mutations in the Type II 3β-Hydroxysteroid Dehydrogenase(3β-HSD) Gene Causing Non-Salt Wasting and Salt Wasting 3β-HSD Deficiency Congenital Adrenal Hyperplasia (CAH) and the Utility of Hormonal Profiles for Diagnosising Bonafide 3β-HSD Deficiency CAH• 505 Pediatric Research, 1998, 43 (Suppl 4) : 89 - 89
- [39] PRODUCTION OF CONGENITAL ADRENAL CORTICAL HYPERPLASIA HYPOSPADIAS AND CLITORAL HYPERTROPHY (ADRENOGENITAL SYNDROME) IN RATS BY INACTIVATION OF 3BETA-HYDROXYSTEROID DEHYDROGENASE PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1966, 121 (03): : 757 - &