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

Neonatal hemolytic anemia due to the mother's rare RhD-/- phenotype: A case report.

Pediatric blood & cancer - 1 Apr 2024

Soleimany Saeed, Shokouhi Iraj, Samare-Najaf Mohammad

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 Anemia, Hemolytic
Share to Infant, Newborn
Share to Mothers
Share to Phenotype

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

Source

Identifiers

PMID: 38235903
DOI: 10.1002/pbc.30877

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 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

Neonatal hemolytic anemia due to the mother's rare RhD-/- phenotype: A case report.PMID 38235903Read ↗

Hemolytic disease of the fetus/newborn: reflections on articles from TRANSFUSION Volume 1.Semantic proximity Read ↗

Successful management of pregnancy and hemolytic disease of the newborn due to anti-HrO in a woman of the D--phenotype.Semantic proximity Read ↗

Review: the molecular basis of the Rh blood group phenotypes.Semantic proximity Read ↗

[Hemolytic diseases in the newborn].Semantic proximity Read ↗

Neonatal Hereditary Spherocytosis: A Case ReportSemantic proximity Read ↗

Haemolytic disease of the newborn: Table 1Semantic proximity Read ↗

Novel RHD variant causing RhD negative phenotype identified in a pregnant woman.Semantic proximity Read ↗

[Hematologic diagnosis of hemolytic disease of the newborn].Semantic proximity Read ↗

Hemolytic disease of the fetus and newborn in the molecular eraSemantic proximity Read ↗

Anti Rh 17 in a multigravida with Rh-D-/[symbol: see text] genotype resulting in haemolytic disease of the newborn.Semantic proximity Read ↗

A Rare Cause of Neonatal Hemolytic Anemia: Glutathione Synthetase Deficiency.Semantic proximity Read ↗

[Neonatal jaundice, hereditary hemolytic anemia].Semantic proximity Read ↗

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