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Article

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

Clinical and experimental obstetrics & gynecology - 1 Jan 1998

Davis S G, Aboud E

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

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Source

Identifiers

PMID: 9856300

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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 Rh 17 in a multigravida with Rh-D-/[symbol: see text] genotype resulting in haemolytic disease of the newborn.PMID 9856300Read ↗

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

[Repeated intrauterine fetal death in a woman with genotype Rh-D-/-D-].Semantic proximity Read ↗

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

Partial D in an obstetrical patient presenting as a mixed field on Rh typing.Semantic proximity Read ↗

A NEW RH PHENOTYPE, RH-0-RH, G-NEGATIVE.Semantic proximity Read ↗

Anti-Rh17 (anti-Hr0): a rare diagnostic and management problem.Semantic proximity Read ↗

D--phenotype due to RHD-RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti-Rh 17(Hrₒ) antibodies.Semantic proximity Read ↗

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

A case of fatal hemolytic disease of the newborn associated with-D-/-D-phenotype.Semantic proximity Read ↗

A new RHD variant allele is caused by a RHD 662C>G mutation.Semantic proximity Read ↗

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

Gene symbol: RHD. Disease: Rhesus negative blood group.Semantic proximity Read ↗

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