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

An overview of molecular diagnosis of steroid 21-hydroxylase deficiency.

The Journal of molecular diagnostics : JMD - 1 May 2001

Keegan C E, Killeen A A

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 Hyperplasia, Congenital
Share to Biochemistry
Share to Blotting, Southern

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

Share to Family Health

Share to Polymorphism, Single-Stranded Conformational

Share to Prenatal Diagnosis

Share to Steroid 21-Hydroxylase

Source

Open in PubMed Open full text

Identifiers

PMID: 11393164
DOI: 10.1016/S1525-1578(10)60651-4
PMCID: PMC1907352

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

An overview of molecular diagnosis of steroid 21-hydroxylase deficiency.PMID 11393164Read ↗

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

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

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

Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiencySemantic proximity Read ↗

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

Routine detection of point mutations in non-classic steroid 21-hydroxylase.Semantic proximity Read ↗

Congenital adrenal hyperplasias.Semantic proximity Read ↗

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

Population-Wide Evaluation of Disease Manifestation in Relation to Molecular Genotype in Steroid 21-Hydroxylase (CYP21) Deficiency: Good Correlation in a Well Defined PopulationSemantic proximity Read ↗

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

Congenital adrenal hyperplasia. Molecular insights learned from patients.Semantic proximity Read ↗

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

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