Circadian variation of plasma 17-hydroxy progesterone among heterozygotic carriers of 21-hydroxylase deficiency (Salt-losing form)

Maria D. Urban, Claude J. Migeon, Peter A. Lee

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

The circadian variation of 17-hydroxyprogesterone levels in 3 male obligatory carriers of 21-hydroxylase deficiency (salt-losing form) was not significantly different from that of normal noncarrier male subjects.

Original languageEnglish (US)
Pages (from-to)74-77
Number of pages4
JournalHormone Research in Paediatrics
Volume23
Issue number2
DOIs
StatePublished - Jan 1 1986

Fingerprint

Progesterone
Salts
17-alpha-Hydroxyprogesterone
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

Cite this

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abstract = "The circadian variation of 17-hydroxyprogesterone levels in 3 male obligatory carriers of 21-hydroxylase deficiency (salt-losing form) was not significantly different from that of normal noncarrier male subjects.",
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Circadian variation of plasma 17-hydroxy progesterone among heterozygotic carriers of 21-hydroxylase deficiency (Salt-losing form). / Urban, Maria D.; Migeon, Claude J.; Lee, Peter A.

In: Hormone Research in Paediatrics, Vol. 23, No. 2, 01.01.1986, p. 74-77.

Research output: Contribution to journalArticle

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