Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Advances in human genetics - 1 Jan 1991

Morel Y, Miller W L

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to 17-alpha-Hydroxyprogesterone
Share to Adrenal Glands
Share to Amniocentesis
Share to Amniotic Fluid

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

Share to Complement C4

Share to Dexamethasone

Share to Gene Conversion

Share to Steroid 21-Hydroxylase

Source

Identifiers

PMID: 1801590
DOI: 10.1007/978-1-4684-5958-6_1

Provenance

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.

Related research

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

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.PMID 1801590Read ↗

Genetics in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and Clinical ImplicationsSemantic proximity Read ↗

21-hydroxylase deficiency congenital adrenal hyperplasia.Semantic proximity Read ↗

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

21-hydroxylase deficiency congenital adrenal hyperplasia.Semantic proximity Read ↗

Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.Semantic proximity Read ↗

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

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.Semantic proximity Read ↗

Congenital adrenal hyperplasias.Semantic proximity Read ↗

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

Congenital adrenal hyperplasia: biochemical and molecular perspectives.Semantic proximity Read ↗

Congenital adrenal hyperplasia due to 21‐hydroxylase deficiencySemantic proximity Read ↗

Congenital Adrenal Hyperplasia (CAH) due to 21-Hydroxylase Deficiency: A Comprehensive Focus on 233 Pathogenic Variants of CYP21A2 Gene.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.