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Article

Genetic basis of endocrine disease 2: congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

The Journal of clinical endocrinology and metabolism - 1 Jan 1992

White P C, New M I

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Share to Adrenal Hyperplasia, Congenital
Share to Chromosome Deletion
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 1727830
DOI: 10.1210/jcem.74.1.1727830

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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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Update on diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiencySemantic proximity Read ↗

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Congenital adrenal hyperplasia: focus on the molecular basis of 21-hydroxylase deficiency.Semantic proximity Read ↗

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