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Article

The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations.

Fertility and sterility - 1 Oct 1999

Escobar-Morreale H F, San Millán J L, Smith R R, Sancho J, Witchel S F

Abstract excerpt

OBJECTIVE: To determine the role of heterozygosity for mutations in the 21-hydroxylase gene (CYP21) in the pathogenesis of hyperandrogenism. DESIGN: Controlled clinical study. SETTING: Tertiary care institutional hospital. PATIENT(S): Forty hirsute women and 13 healthy control women. INTERVENTION(S): The source of androgen excess was determined by the changes in serum testosterone levels in response to a single...

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Source

Identifiers

PMID: 10521100
DOI: 10.1016/s0015-0282(99)00317-9

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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