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

Identification of a novel B allele with a nucleotide deletion (c.103_106 delG) in the ABO gene associated with a B weak phenotype.

Transfusion - 1 Mar 2021

He Yunlei, Yu Lu, Xu Deyi, Zhang Jiwei, Deng Gang

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 Alleles
Share to Asian People
Share to Exons

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

Share to Genotype

Share to Haplotypes

Share to Phenotype

Share to Sequence Deletion

Source

Identifiers

PMID: 33615482
DOI: 10.1111/trf.16302

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 17 Oct 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

Identification of a novel B allele with a nucleotide deletion (c.103_106 delG) in the ABO gene associated with a B weak phenotype.PMID 33615482Read ↗

ABO*B.01+c.464A>C represents a missense variation in the ABO gene and encodes a weak B phenotype.Semantic proximity Read ↗

Identification of a novel B allele with missense mutation (c.98G > C) in the ABO gene.Semantic proximity Read ↗

Identification of a novel B allele with a c.586T>C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel B allele with a c.256G>A mutation on the ABO*B.01 allele.Semantic proximity Read ↗

Identification of a novel B allele with a c.917 T > C mutation on the ABO*B.01 allele.Semantic proximity Read ↗

A novel B variant allele with c.586T>C (p.Cys196Arg) mutation identified at the ABO locus.Semantic proximity Read ↗

Identification of a novel A allele with a nucleotide deletion c.198delG in the ABO gene associated with Ael phenotype.Semantic proximity Read ↗

A novel variant B allele at the ABO gene locus characterized by a duplication-based insertion of 27 nucleotides identified in an Iraqi male with a weak B subgroup phenotype.Semantic proximity Read ↗

Identification of a novel A allele with initiator codon variant (c.2T > A) in the ABO gene associated with weak A phenotype.Semantic proximity Read ↗

Identification of a novel A allele with a nucleotide insert (c.99-1_100 T) in the ABO gene associated with a A3 phenotype individual.Semantic proximity Read ↗

Identification of novel variant B alleles within the ABO gene.Semantic proximity Read ↗

Identification of a novel A allele with a c.36-39delA on the ABO*A1.02 allele.Semantic proximity Read ↗

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