Document Detail


The Jk(a-b-) phenotype in New Zealand Polynesians.
MedLine Citation:
PMID:  7101419     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The Kidd locus phenotype Jk(a-b-) was detected in 0.9 percent of Polynesians living in New Zealand. Over a period of 13 years, nine examples of anti-Jk3 were detected, one of which caused a delayed hemolytic transfusion reaction. Other examples resulted in mild hemolytic disease of the newborn. The anti-Jk3 reacted as an inseparable antibody, confirmed that inheritance of the Jk(a-b-) phenotype was best explained by the presence of a silent Jk allele.
Authors:
D G Woodfield; R Douglas; J Smith; A Simpson; L Pinder; J M Staveley
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Transfusion     Volume:  22     ISSN:  0041-1132     ISO Abbreviation:  Transfusion     Publication Date:    1982 Jul-Aug
Date Detail:
Created Date:  1982-09-10     Completed Date:  1982-09-10     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0417360     Medline TA:  Transfusion     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  276-8     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Alleles
Blood Group Antigens / genetics*
Blood Group Incompatibility / immunology
Child
Erythroblastosis, Fetal / immunology
European Continental Ancestry Group*
Female
Humans
Infant, Newborn
Kidd Blood-Group System / genetics*,  immunology
New Zealand
Phenotype*
Polynesia / ethnology
Pregnancy
Chemical
Reg. No./Substance:
0/Blood Group Antigens; 0/Kidd Blood-Group System

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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