Male pseudohermaphroditism due to 17α-hydroxylase deficiency
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Cited by 237 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
1. Congenital Adrenal Hyperplasia with Combined 21-hydroxylase deficiency and 17α-hydroxylase/17,20-lyase deficiency: An undervirilized male;European Journal of Medical Genetics;2024-06
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3. Diagnosis of 17-alpha hydroxylase deficiency performed late in life in a patient with a 46,XY karyotype;Endocrinology, Diabetes & Metabolism Case Reports;2023-04-01
4. Severe hypertension caused by 17α-hydroxylase deficiency: A case report;Heliyon;2023-03
5. Presentation, Diagnosis, and Follow-Up Characteristics of 17α-Hydroxylase Deficiency Cases with Exon 1–6 Deletion (Founder Mutation) in the CYP17A1Gene: 20-Year Single-Center Experience;Sexual Development;2023
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