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

[The Ko phenotype and fetal-maternal allo-immunization].

Archives francaises de pediatrie - 1 Nov 1993

Fourmaintraux A, Vitrac D, Mariette J B, Brunel F

Abstract excerpt

BACKGROUND: Very few people have no Kell antigens (phenotype Ko). They can develop antibodies to Kell antigens after transfusion, or the abortion of a Kell-positive fetus. This paper describes a case of immunization that may have been due to amniocentesis. CASE REPORT: The eighth pregnancy of a woman required an amniocentesis on the 17th week for chromosomal study because she was 41 years old. She had 4 prior...

Read the complete abstract on PubMed

Topics

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

Share to Amniocentesis
Share to Immunization
Share to Infant, Newborn

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

Share to Kell Blood-Group System

Share to Maternal-Fetal Exchange

Share to Pedigree

Share to Phenotype

Share to Pregnancy

Source

Identifiers

PMID: 8060208

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

[The Ko phenotype and fetal-maternal allo-immunization].PMID 8060208Read ↗

[Anti-K antibodies in pregnant women and genotyping of K antigen in foetuses].Semantic proximity Read ↗

Distribution of Kell phenotype among pregnant women in Sokoto, North Western Nigeria.Semantic proximity Read ↗

Kell and Kx blood group systems.Semantic proximity Read ↗

Possible suppression of fetal erythropoiesis by the Kell blood group antibody anti-Kp(a).Semantic proximity Read ↗

[A KEL*02mod allele responsible for an apparent maternity exclusion].Semantic proximity Read ↗

[Prenatal typing of Rh- and Kell- blood group system antigens].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 ↗

Alloantibodies to a paternally derived RBC KEL antigen lead to hemolytic disease of the fetus/newborn in a murine modelSemantic proximity Read ↗

Molecular basis of the Kell-null phenotype: a mutation at the splice site of human KEL gene abolishes the expression of Kell blood group antigens.Semantic proximity Read ↗

[Perinatal hemolytic disease. Part 1: physiopathology].Semantic proximity Read ↗

[The Identification Idea of Antibodies Against Ku and Other High-Frequency Antigens].Semantic proximity Read ↗

Anti-Ku alloimmunization due to a KEL*02N.19 allele causing Kell-null phenotype despite KEL*02 genotype prediction.Semantic proximity Read ↗

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