5 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 30614301 | A new compound heterozygous mutation in a female with 17α-hydroxylase/17,20-lyase deficiency, slipped capital femoral epiphysis, and adrenal myelolipoma. | 2019 May | 2 |
2 | 31515780 | [Analysis of CYP17A1 gene variants in 5 patients with 17-hydroxylase deficiency]. | 2019 Sep 10 | 1 |
3 | 31695722 | A Novel Compound Heterozygous CYP17A1 Variant Causes 17α-Hydroxylase/17, 20-Lyase Deficiency. | 2019 | 3 |
4 | 30695673 | Two novel heterozygous mutations in the CYP17A1 gene in a Chinese patient with 17α-hydroxylase 17,20-lyase deficiency. | 2018 Dec | 3 |
5 | 19040066 | [A clinical and genetic analysis of a pedigree with two 46,XY patients suffering from 17alpha-hydroxylase deficiency]. | 2008 Jun | 3 |