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 case of Am, a rare variant in the ABO blood group system.

Haematologica - 1 Jan 2000

Galiano L, Veratti A, Iiritano E, Colicigno G, Senatore C

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 ABO Blood-Group System
Share to Aged
Share to Agglutination Tests
Share to ABO gene

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

Share to Genetic Variation

Share to Phenotype

Source

Identifiers

PMID: 3096826

Genes

ABO

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A case of Am, a rare variant in the ABO blood group system.PMID 3096826Read ↗

[ABO blood-group system: past and present].Semantic proximity Read ↗

Anomalous ABO phenotype in a child after an ABO-incompatible liver transplantation.Semantic proximity Read ↗

[Unusual cis AB phenotype in ABO group system].Semantic proximity Read ↗

Molecular genetic analysis for a novel Ael allele of the ABO blood group system.Semantic proximity Read ↗

Molecular genetic analysis of the Am phenotype of the ABO blood group system.Semantic proximity Read ↗

ABO gene mutation c.815_816insG in an African individual forms a novel Ael allele.Semantic proximity Read ↗

The Augustine blood group system, 48 years in the making.Semantic proximity Read ↗

[AEL: a rare variant of blood group A].Semantic proximity Read ↗

[Association of hemoglobin O Arab/ hemoglobin S: 3 cases].Semantic proximity Read ↗

A novel mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a blood donor with the Am B phenotype.Semantic proximity Read ↗

A novel A allele with 664G>A mutation identified in a family with the Am phenotype.Semantic proximity Read ↗

[B0 aberrant genotype of AB0 blood group system].Semantic proximity Read ↗

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