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4. A Novel Heterozygous Mutation of the CYP17A1 Gene in a Child with a Micropenis and Isolated 17,20-Lyase Deficiency
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7. 46,XY Disorder of Sex Development Caused by 17α-Hydroxylase/17,20-Lyase Deficiency due to Homozygous Mutation ofCYP17A1Gene: Consequences of Late Diagnosis
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8. Refractory hypokalemia with sexual dysplasia and infertility caused by 17α-hydroxylase deficiency and triple X syndrome: A case report
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13. Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report
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14. Cytochrome P450 family 17 subfamily A member 1 mutation causes severe pseudohermaphroditism: A case report
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15. 17-Alpha-Hydroxylase Deficiency
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16. Partial deficiency of 17α-hydroxylase: a rare cause of congenital adrenal hyperplasia
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17. Adrenal Gland Therapies
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19. Selective LC-MRM/SIM-MS based profiling of adrenal steroids reveals metabolic signatures of 17α-hydroxylase deficiency
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20. Two Cases with 17-alpha Hydroxylase Deficiency Misdiagnosed as Primary Aldosteronism
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21. 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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23. 17 alpha‐hydroxylase deficiency: A case report of young Chinese woman with a rare gene mutation
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