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

Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden.

Blood transfusion = Trasfusione del sangue - 1 Sept 2024

Pardi Cecilia, Hellberg Åsa, Isakson Pauline

Abstract excerpt

BACKGROUND: The Rh blood group system is highly complex, polymorphic, and immunogenic. The presence of RHD gene variants in RhD negative pregnant women is a challenge in fetal RHD genotyping as it may influence the antenatal management of anti-D prophylaxis. The aim of this study was to determine the efficiency of a non-invasive single-exon approach in the obstetric population of Western Sweden in a 31-month...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Exons
Share to Follow-Up Studies
Share to Genotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotyping Techniques

Share to Infant, Newborn

Share to Pregnancy

Share to Rh-Hr Blood-Group System

Share to Sweden

Source

Open in PubMed Open full text

Identifiers

PMID: 38814881
DOI: 10.2450/BloodTransfus.741
PMCID: PMC11390609

Genes

RHD

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

Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden.PMID 38814881Read ↗

Evaluation of an automated platform for non-invasive single-exon fetal RHD genotyping early in pregnancy.Semantic proximity Read ↗

Investigation of discrepancies obtained during 15 years of non-invasive fetal RHD genotyping in apparent serologic RhD-negative pregnant women.Semantic proximity Read ↗

Single-exon approach to non-invasive fetal RHD screening in early pregnancy: An update after 10 years' experience.Semantic proximity Read ↗

Routine noninvasive prenatal screening for fetal Rh D in maternal plasma-A 2-year experience from a single center in Belgium.Semantic proximity Read ↗

Prenatal RHD genotyping in Croatia: preliminary results.Semantic proximity Read ↗

Noninvasive Single-Exon Fetal RHD Determination in a Routine Screening Program in Early PregnancySemantic proximity Read ↗

Terminating Routine Cord Blood RhD Typing of the Newborns to Guide Postnatal Anti-D Immunoglobulin Prophylaxis Based on the Results of Fetal RHD Genotyping.Semantic proximity Read ↗

Routine fetal RHD genotyping with maternal plasma: a four-year experience in Belgium.Semantic proximity Read ↗

Diagnostic accuracy of noninvasive fetal Rh genotyping from maternal blood--a meta-analysis.Semantic proximity Read ↗

Diagnostic accuracy of non-invasive fetal RhD genotyping using cell-free fetal DNA: a meta analysisSemantic proximity Read ↗

Non-Invasive Prenatal Fetal Blood Group Genotype and Its Application in the Management of Hemolytic Disease of Fetus and Newborn: Systematic Review and Meta-Analysis.Semantic proximity Read ↗

Prenatal non-invasive foetal RHD genotyping: diagnostic accuracy of a test as a guide for appropriate administration of antenatal anti-D immunoprophylaxis.Semantic proximity Read ↗

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