| 1 |
32945709 | A rare intronic mutation in the splice acceptor site of the CYP17A1 gene in a patient with 17α-hydroxylase/17,20-lyase deficiency. | 2021 Jan |
1 |
| 2 |
31464148 | A report of congenital adrenal hyperplasia due to 17α-hydroxylase deficiency in two 46,XX sisters. | 2020 Jan |
1 |
| 3 |
26862015 | Steroid 17-hydroxylase and 17,20-lyase deficiencies, genetic and pharmacologic. | 2017 Jan |
2 |
| 4 |
19454579 | Steroid 17alpha-hydroxylase deficiency: functional characterization of four mutations (A174E, V178D, R440C, L465P) in the CYP17A1 gene. | 2009 Aug |
1 |
| 5 |
20021817 | [Genetic mutation analysis of a kindred with a patient suffering from 17 alpha-hydroxylase/17, 20-lyase deficiency]. | 2009 Oct |
1 |
| 6 |
7629254 | Seventeen alpha-hydroxylase deficiency with one base pair deletion of the cytochrome P450c17 (CYP17) gene. | 1995 Aug |
2 |