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[Classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Genetic considerations in light of personal studies].

Przeglad lekarski - 1 Jan 1995

Turowska-Heydel D

Abstract excerpt

Long-term immunogenetic studies on HLA and GLOI systems in the families of probands with classic 21-hydroxylase related adrenal hyperplasia served as a basis for a complex analysis. The analyzed factors included the phenotype and haplotype incidence, HLA-ABC homozygosity, and -in informational families-the strength of genetic linkage for recombinant fractions (lod score). The results suggest the usefulness of...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 7784603

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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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[Classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Genetic considerations in light of personal studies].PMID 7784603Read ↗

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[Congenital dysfunction of adrenal cortex - detection of new mutant gene of 21-hydroxylase].Semantic proximity Read ↗

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Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).Semantic proximity Read ↗

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