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Article

[Current data on the molecular biology of 21-hydroxylase deficiency. Diagnostic applications].

Archives francaises de pediatrie - 1 Jan 1992

Mornet E, Boué J, Crète P, Raux-Demay M C, Kutten F, Boué A

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Share to Adrenal Hyperplasia, Congenital
Share to DNA Probes, HLA
Share to Infant, Newborn
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Steroid 21-Hydroxylase

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PMID: 1550455

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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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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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[Current data on the molecular biology of 21-hydroxylase deficiency. Diagnostic applications].PMID 1550455Read ↗

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An overview of molecular diagnosis of steroid 21-hydroxylase deficiency.Semantic proximity Read ↗

[11Beta-hydroxylase deficiency].Semantic proximity Read ↗

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[Localization of the pathologic gene for 21-hydroxylase enzyme deficiency within the HLA system].Semantic proximity Read ↗

[Consensus on laboratory diagnosis of congenital adrenal hyperplasia due to 21 hydroxylase deficiency].Semantic proximity Read ↗

Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.Semantic proximity Read ↗

[17alpha-hydroxylase/17,20lyase deficiency].Semantic proximity Read ↗

[Adrenal enzyme deficiency].Semantic proximity Read ↗

Molecular Diagnosis of Steroid 21-Hydroxylase Deficiency: A Practical Approach.Semantic proximity Read ↗

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