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

Lack of RH C/E expression in the Rhesus D--phenotype is the result of a gene deletion.

Annals of human genetics - 1 Jan 1994

Blunt T, Steers F, Daniels G, Carritt B

Abstract excerpt

We have investigated the arrangement of genes in the rare Rh (Rhesus) partial null condition D--. Southern blot and PCR studies under conditions which distinguish the highly homologous RH D and RH C/E genes show that in an Icelandic family with the D-- haplotype at least 85% of the RH C/E gene is deleted. This finding is in contrast to one other published case of this phenotype, where intact RH D and C/E genes...

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to Exons
Share to Heterozygote

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

Share to Homozygote

Share to Molecular Sequence Data

Share to Phenotype

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Source

Identifiers

PMID: 7913307
DOI: 10.1111/j.1469-1809.1994.tb00722.x

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

Lack of RH C/E expression in the Rhesus D--phenotype is the result of a gene deletion.PMID 7913307Read ↗

Structure and expression of the RH locus in the Rh-deficiency syndrome.Semantic proximity Read ↗

Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background.Semantic proximity Read ↗

A recombination hot spot in the Rh genes revealed by analysis of unrelated donors with the rare D-- phenotype.Semantic proximity Read ↗

Identification of a partial internal deletion in the RH locus causing the human erythrocyte D--phenotype.Semantic proximity Read ↗

Rh null phenotypes are not due to a gross deletion and can occur on different Rh genetic backgrounds.Semantic proximity Read ↗

A novel nonsense variant in RHAG underlies a Nordic Rhnull phenotype.Semantic proximity Read ↗

RH blood group system and molecular basis of Rh-deficiency.Semantic proximity Read ↗

Characterization of the recombination hot spot involved in the genomic rearrangement leading to the hybrid D-CE-D gene in the D(VI) phenotype.Semantic proximity Read ↗

Three unrelated Rh D gene polymorphisms identified among blood donors with Rhesus CCee (r'r') phenotypes.Semantic proximity Read ↗

Rhnull syndrome: identification of a novel mutation in RHce.Semantic proximity Read ↗

Molecular defects of the RHCE gene in Rh-deficient individuals of the amorph type.Semantic proximity Read ↗

Molecular biology of partial D phenotypes.Semantic proximity Read ↗

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