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

A polymorphic poly-A sequence in the 5' region of the aldosynthase (CYP11B2) gene may be useful in genetic diagnosis of 11 beta-hydroxylase genes defects.

Human genetics - 1 Sept 1994

Clot F, Jager M, Simon-Bouy B, Serre J L, Aupetit-Faisant B, Mornet E

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 Adrenal Hyperplasia, Congenital
Share to Cytochrome P-450 CYP11B2
Share to Cytochrome P-450 Enzyme System

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Primers

Share to Gene Frequency

Share to Poly A

Share to Polymerase Chain Reaction

Share to Steroid 11-beta-Hydroxylase

Source

Identifiers

PMID: 8076952
DOI: 10.1007/BF00208293

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A polymorphic poly-A sequence in the 5' region of the aldosynthase (CYP11B2) gene may be useful in genetic diagnosis of 11 beta-hydroxylase genes defects.PMID 8076952Read ↗

Polymorphisms of Human Aldehyde DehydrogenasesSemantic proximity Read ↗

Heterozygosity for the Novel HBA2: c.*91_*92delTA Polyadenylation Site Variant on the α2-Globin Gene Expanding the Genetic Spectrum of α-Thalassemia in Iran.Semantic proximity Read ↗

Association of a new polymorphism in ALOX12 gene with bipolar disorder.Semantic proximity Read ↗

Haemoglobin H hydrops fetalis syndrome associated with homozygosity for the alpha2-globin gene polyadenylation signal mutation AATAAA-->AATA- -.Semantic proximity Read ↗

Identification of a novel a variant at the ABO locus in Chinese Han individuals with a A2 phenotype.Semantic proximity Read ↗

[The allele A1 at the DRD2 locus on chromosome 11--genetic marker for alcoholism].Semantic proximity Read ↗

Studies on the dominant negative effect of the ALDH2*2 allele.Semantic proximity Read ↗

Homozygosity for the AATAAA > AATA- - Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian Patient: A Case Report.Semantic proximity Read ↗

Molecular evaluation of an Alu repeat including a polymorphic variable poly(dA) (AluVpA) in the vitamin D binding protein (DBP) gene.Semantic proximity Read ↗

Unusual length polymorphism in human steroid 5 alpha-reductase type 2 gene (SRD5A2).Semantic proximity Read ↗

Characterization of polymorphisms at the 11 beta-hydroxylase (CYP11B1) locus.Semantic proximity Read ↗

G/T polymorphism in CRYA2 gene.Semantic proximity Read ↗

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