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17 alpha- hydroxylase deficiency
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OMIM - Congenital disorder
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Analysis of CYP17A1 gene mutation in a child patient with 17 alpha-hydroxylase/17, 20-lyase deficien…
Delayed puberty from partial 17-alpha hydroxylase enzyme deficiency.
Diagnosis and treatment of 17 alpha-hydroxylase deficiency: a case report and literature review].
17-alpha-hydroxylase deficiency: a case report with clinical and molecular analysis.
New compound heterozygous mutation causes partial combined 17 alpha-hydroxylase/17,20-lyase deficien…
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Vitamin D Deficiency Treatment Outcomes After Non-ST-Segment Elevation Myocardial Infarction
Suspected Deficient Activation of Vitamin D in Patients With Secondary Hyperparathyroidism
Pharmacogenetics of Metformin Action in PCOS
Influence of Kidney Performance and Magnesium on Formation of (OH)2-vitamin D3
Cholecalciferol (Vitamin D3) Therapy in Chronic Kidney Disease (CKD) Subjects
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