1. A rare case of 17α-hydroxylase/17, 20-lyase deficiency: Clinical and genetic findings and follow-up outcomes
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2. Cytochrome P450 family 17 subfamily A member 1 mutation causes severe pseudohermaphroditism: A case report
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3. The Role of Biomarkers in Adrenocortical Carcinoma: A Review of Current Evidence and Future Perspectives
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5. Partial deficiency of 17α-hydroxylase: a rare cause of congenital adrenal hyperplasia
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6. Case report: 17α− hydroxylase deficiency due to a hotspot variant and a novel compound heterozygous variant in the CYP17A1 gene of five Chinese patients
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7. A Novel Heterozygous Mutation of the CYP17A1 Gene in a Child with a Micropenis and Isolated 17,20-Lyase Deficiency
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8. Prior to versus after Metformin Treatment—Effects on Steroid Enzymatic Activities
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9. Adrenal Gland Therapies
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10. 46,XY Disorder of Sex Development Caused by 17α-Hydroxylase/17,20-Lyase Deficiency due to Homozygous Mutation ofCYP17A1Gene: Consequences of Late Diagnosis
    Giampaolo Papi et al, 2018, Case Reports in Endocrinology CrossRef
11. Refractory hypokalemia with sexual dysplasia and infertility caused by 17α-hydroxylase deficiency and triple X syndrome: A case report
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12. Reproductive endocrine characteristics and in vitro fertilization treatment of female patients with partial 17α-hydroxylase deficiency: Two pedigree investigations and a literature review
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13. Selective LC-MRM/SIM-MS based profiling of adrenal steroids reveals metabolic signatures of 17α-hydroxylase deficiency
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14. Two Cases with 17-alpha Hydroxylase Deficiency Misdiagnosed as Primary Aldosteronism
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15. Endocrine and Immune System Disorders
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16. An integrative literature review of menstruation patterns in people with congenital adrenal hyperplasia
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17. Successful live birth in women with partial 17α-hydroxylase deficiency: report of two cases
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18. Phthalate Exposures and Placental Health in Animal Models and Humans: A Systematic Review
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19. Genetic diagnosis and clinical analysis of 17α-hydroxylase/17, 20-lyase deficiency combined with type 2 diabetes mellitus: A case report
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20. Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report
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21. Multiplexed Serum Steroid Profiling Reveals Metabolic Signatures of Subtypes in Congenital Adrenal Hyperplasia
    Jaeyoon Shim et al, 2023, Journal of the Endocrine Society CrossRef
22. 17 alpha‐hydroxylase deficiency: A case report of young Chinese woman with a rare gene mutation
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23. Environmental enrichment improves social isolation-induced memory impairment: The possible role of ITSN1-Reelin-AMPA receptor signaling pathway
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24. How Is CYP17A1 Activity Altered in Autism? A Pilot Study to Identify Potential Pharmacological Targets
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