Transfusion
Article . 2010 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
Novel IVS6‐13C>T mutation recognized as a cause of discrepancy between phenotyping and genotyping in KEL*3,4 polymorphism identification
Authors: Edmir, Boturão-Neto; Akemi K, Chiba; José O, Bordin;
pmid: 20609202
Novel IVS6‐13C>T mutation recognized as a cause of discrepancy between phenotyping and genotyping in KEL*3,4 polymorphism identification
Related Organizations
- UNIVERSIDADE DE SAO PAULO Brazil
- Universidade de São Paulo Brazil
Keywords
Male, Genotype, Kell Blood-Group System, Mutation, Missense, Humans, Female, Brazil, Polymorphism, Restriction Fragment Length
Male, Genotype, Kell Blood-Group System, Mutation, Missense, Humans, Female, Brazil, Polymorphism, Restriction Fragment Length
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citations
Citations provided by BIP!
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
popularity
Popularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
0
Average
Average
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