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

Anti-D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn.

Transfusion - 1 Aug 2017

Quantock Kelli M, Lopez Genghis H, Hyland Catherine A, Liew Yew-Wah, Flower Robert L, Niemann Frans J, Joyce Arthur

Abstract excerpt

BACKGROUND: Individuals with the partial D phenotype when exposed to D+ red blood cells (RBCs) carrying the epitopes they lack may develop anti-D specific for the missing epitopes. DNB is the most common partial D in Caucasians and the clinical significance for anti-D in these individuals is unknown. STUDY DESIGN AND METHODS: This article describes the serologic genotyping results and clinical manifestations in...

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 Erythroblastosis, Fetal

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

Share to Fetal Diseases

Share to Mothers

Share to Rh-Hr Blood-Group System

Share to Rh Isoimmunization

Share to Rho(D) Immune Globulin

Source

Identifiers

PMID: 28639307
DOI: 10.1111/trf.14156

Genes

RHD

Variants

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

Anti-D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn.PMID 28639307Read ↗

Two cases of the variant RHD*DAU5 allele associated with maternal alloanti-D.Semantic proximity Read ↗

RHD alleles among pregnant women with serologic discrepant weak D phenotypes from a multiethnic population and risk of alloimmunization.Semantic proximity Read ↗

A Korean family with RHD*DNT only detectable after anti-D alloimmunization.Semantic proximity Read ↗

Fatal hydrops fetalis caused by anti-D in a mother with partial DSemantic proximity Read ↗

Molecular and serologic characterization of DWI, a novel "high-grade" partial D.Semantic proximity Read ↗

Cases of RhD variants RhD*DAU2/DAU6 and RhD*weak D type 4.1 in pregnant women in Saudi Arabia.Semantic proximity Read ↗

Anti-D alloimmunisation in pregnant women with DEL phenotype in China.Semantic proximity Read ↗

Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention.Semantic proximity Read ↗

Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles.Semantic proximity Read ↗

Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture.Semantic proximity Read ↗

Haemolytic disease of the fetus and newbornSemantic proximity Read ↗

Development of anti-D in a severe delayed hemolytic transfusion reaction due to DAU3, a partial D variant allele.Semantic proximity Read ↗

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