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

Prenatal diagnosis of Kell blood group genotypes: KEL1 and KEL2.

American journal of obstetrics and gynecology - 1 Aug 1996

Lee S, Bennett P R, Overton T, Warwick R, Wu X, Redman C M

Abstract excerpt

OBJECTIVE: Our purpose was to devise diagnostic test(s) that determine fetal KEL1 and KEL2 genotypes. STUDY DESIGN: KEL1 and KEL2 polymorphisms are due to a single C to T base substitution at nucleotide 698 of exon 6 of KEL. This allowed us to develop two polymerase chain reaction tests that distinguish KEL1/1 and KEL2/2 homozygotes and KEL1/2 heterozygotes. The first test uses a Bsm I restriction fragment length...

Read the complete abstract on PubMed

Topics

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

Share to Genotype
Share to Base Sequence
Share to DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Erythrocytes

Share to Molecular Sequence Data

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Share to Prenatal Diagnosis

Source

Identifiers

PMID: 8765268
DOI: 10.1016/s0002-9378(96)70161-8

Genes

KEL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Prenatal diagnosis of Kell blood group genotypes: KEL1 and KEL2.PMID 8765268Read ↗

Prenatal determination of genotypes Kell and Cellano in at-risk pregnancies.Semantic proximity Read ↗

Genotyping of KEL1 and KEL2 of the human Kell blood group system by the polymerase chain reaction with sequence-specific primers.Semantic proximity Read ↗

KEL*02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,-2 phenotypes.Semantic proximity Read ↗

An innovative test for non-invasive Kell genotyping on circulating fetal DNA by means of the allelic discrimination of K1 and K2 antigens.Semantic proximity Read ↗

Next-generation sequencing: proof of concept for antenatal prediction of the fetal Kell blood group phenotype from cell-free fetal DNA in maternal plasma.Semantic proximity Read ↗

Molecular basis of Kell blood group phenotypes.Semantic proximity Read ↗

A KEL gene encoding serine at position 193 of the Kell glycoprotein results in expression of KEL1 antigen.Semantic proximity Read ↗

Molecular basis of the Kell (K1) phenotype.Semantic proximity Read ↗

Development of a PCR-based diagnostic assay for the determination of KEL genotype in donor blood samples.Semantic proximity Read ↗

Noninvasive diagnostics of fetal KEL*01.01 allele from maternal plasma of immunized women using digital PCR protocols.Semantic proximity Read ↗

Point mutations in KEL exon 8 determine a high-incidence (RAZ) and a low-incidence (KEL25, VLAN) antigen of the Kell blood group system.Semantic proximity Read ↗

The Kell blood group system.Semantic proximity Read ↗

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