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Arch Dis Child. 1968 August; 43(230): 410–414.
PMCID: PMC2019993

Evaluation of deficiency of 21-hydroxylation in patients with congenital adrenal hyperplasia.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • BONGIOVANNI AM. Adrenogenital syndrome: uncomplicated and hypertensive forms. Pediatrics. 1958 Apr;21(4):661–667. [PubMed]
  • BONGIOVANNI AM, ROOT AW. The adrenogenital syndrome. N Engl J Med. 1963 Jun 13;268:1342–contd. [PubMed]
  • JACOBS DR, VAN DER POLL J, GABRILOVE JL, SOFFER LJ. 17alpha-Hydroxyprogesterone--a salt-losing steroid: relation to congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1961 Aug;21:909–922. [PubMed]
  • KOWARSKI A, FINKELSTEIN JW, SPAULDING JS, HOLMAN GH, MIGEON CJ. ALDOSTERONE SECRETION RATE IN CONGENITAL ADRENAL HYPERPLASIA. A DISCUSSION OF THE THEORIES ON THE PATHOGENESIS OF THE SALT-LOSING FORM OF THE SYNDROME. J Clin Invest. 1965 Sep;44:1505–1513. [PMC free article] [PubMed]
  • SILBER RH, PORTER CC. The determination of 17,21-dihydroxy-20-ketosteroids in urine and plasma. J Biol Chem. 1954 Oct;210(2):923–932. [PubMed]
  • ULICK S, GAUTIER E, VETTER KK, MARKELLO JR, YAFFE S, LOWE CU. AN ALDOSTERONE BIOSYNTHETIC DEFECT IN A SALT-LOSING DISORDER. J Clin Endocrinol Metab. 1964 Jul;24:669–672. [PubMed]

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