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

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

Blood - 15 Jul 1995

Huang C H, Reid M E, Chen Y

Abstract excerpt

The D--phenotype of the human erythrocyte is a genetic variant of the Rh blood group system associated with the expression of D but not C, c, E, and e (designated non-D) antigens. In this report, we characterize the structure and expression of Rh polypeptide genes in two D--homozygotes of Italian origin. Southern blot analysis detected a gross deletion in their genomic DNA that correlated with the alteration of...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Base Sequence
Share to DNA, Complementary

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

Share to DNA Mutational Analysis

Share to Homozygote

Share to Molecular Sequence Data

Share to Phenotype

Source

Identifiers

PMID: 7606008

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

Identification of a partial internal deletion in the RH locus causing the human erythrocyte D--phenotype.PMID 7606008Read ↗

Human D(IIIa) erythrocytes: RhD protein is associated with multiple dispersed amino acid variations.Semantic proximity Read ↗

Molecular cloning and primary structure of the human blood group RhD polypeptide.Semantic proximity Read ↗

Recent advances in molecular and genetic analysis of Rh blood group structures.Semantic proximity Read ↗

RhD variant caused by an in-frame triplet duplication in the RHD gene.Semantic proximity Read ↗

Isolation, characterization, and family study of DTI, a novel partial D phenotype affecting the fourth external loop of D polypeptides.Semantic proximity Read ↗

Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene.Semantic proximity Read ↗

Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms.Semantic proximity Read ↗

Alteration of RH gene structure and expression in human dCCee and DCW-red blood cells: phenotypic homozygosity versus genotypic heterozygosity.Semantic proximity Read ↗

In-frame triplet deletions in RHD alter the D antigen phenotype.Semantic proximity Read ↗

Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals.Semantic proximity Read ↗

The serological profile and molecular basis of a new partial D phenotype, DHR.Semantic proximity Read ↗

Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis.Semantic proximity Read ↗

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