Congenital Adrenal Hyperplasia - Endotext - NCBI Bookshelf
Primary amenorrhoea with hypertension: undiagnosed 17-α-hydroxylase deficiency | The Medical Journal of Australia
Rat Steroid 17-alpha-hydroxylase/17,20 lyase (CYP17a1) ELISA Kit | Abbexa Ltd
![PDF] A case of 17 alpha-hydroxylase deficiency | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/572852497019db8cfa6066351eae8429a30b6d1a/2-Figure1-1.png "PDF] A case of 17 alpha-hydroxylase deficiency | Semantic Scholar")
PDF] A case of 17 alpha-hydroxylase deficiency | Semantic Scholar
17-Hydroxylase Deficiency Syndrome: Background, Pathophysiology, Etiology
Adrenogenital Syndrome (Congenital Adrenal Hyperplasia) - Endocrine - Medbullets Step 1
Schematic of the adrenal steroidogenesis biosynthesis pathway. HSD,... | Download Scientific Diagram
17α-Hydroxylase Deficiency is an Underdiagnosed Disease: High Frequency of Misdiagnoses in a Large Cohort of Brazilian Patients - Endocrine Practice
Figure 1 from A successful live birth from a 17 α-hydroxylase / 17 , 20-lyase deficiency mother by the in vitro fertilization frozen-thawed embryo transfer | Semantic Scholar
Development of abiraterone acetate, a 17-alpha hydroxylase C17,20-lyase inhibitor as a secondary hormonal therapy in prostate cancer - ScienceDirect
17-Hydroxylase Deficiency Syndrome: Background, Pathophysiology, Etiology
Steroid 17-hydroxylase and 17,20-lyase deficiencies, genetic and pharmacologic - ScienceDirect
Genetic causes of rare forms of congenital adrenal hyperplasia
Oman Medical Journal-Archive
17 alpha-hydroxylase deficiency pathophysiology - wikidoc
![PDF] 17α-hydroxylase/17,20-lyase deficiency in congenital adrenal hyperplasia: A case report | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/179a0a7d72de80798d8dffe8c3069db09dcc3504/4-Figure2-1.png "PDF] 17α-hydroxylase/17,20-lyase deficiency in congenital adrenal hyperplasia: A case report | Semantic Scholar")
PDF] 17α-hydroxylase/17,20-lyase deficiency in congenital adrenal hyperplasia: A case report | Semantic Scholar
![PDF] Congenital Adrenal Hyperplasia due to 17-alpha-hydoxylase/17,20-lyase Deficiency Presenting with Hypertension and Pseudohermaphroditism: First Case Report from Oman. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/2a646a6f0e4f6a2b29a89cc11672ce99c859d57a/2-Figure1-1.png "PDF] Congenital Adrenal Hyperplasia due to 17-alpha-hydoxylase/17,20-lyase Deficiency Presenting with Hypertension and Pseudohermaphroditism: First Case Report from Oman. | Semantic Scholar")
PDF] Congenital Adrenal Hyperplasia due to 17-alpha-hydoxylase/17,20-lyase Deficiency Presenting with Hypertension and Pseudohermaphroditism: First Case Report from Oman. | Semantic Scholar
JCM | Free Full-Text | Pregnancy and Prenatal Management of Congenital Adrenal Hyperplasia
KEGG REACTION: R08517
17-Hydroxylase Deficiency Syndrome: Background, Pathophysiology, Etiology
Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report | Journal of Medical Case Reports | Full Text
1.14.14.19: steroid 17alpha-monooxygenase - BRENDA Enzyme Database
