Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.
about
Molecular Basis of KELnull Phenotype in Brazilians.The value of DNA analysis for antigens of the Kell and Kx blood group systems.Genetic and functional analyses describe a novel 730delG mutation in the KEL gene causing K0 phenotype in a Taiwanese blood donor.Silent KEL alleles identified from Japanese individuals with the Ko phenotype.Three uncommon KEL alleles in one family with unusual Kell phenotypes explain a 35-year old conundrum.Identification of novel silent KEL alleles causing KEL:-5 (Ko) phenotype or discordance between KEL:1,-2 phenotype/KEL*01/02 genotype.Genetic diversity of KELnull and KELel: a nationwide Austrian survey.Serial blood donations for intrauterine transfusions of severe hemolytic disease of the newborn with the use of recombinant erythropoietin in a pregnant woman alloimmunized with anti-Ku.
P2860
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P2860
Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.
description
2002 nî lūn-bûn
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2002年の論文
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2002年学术文章
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name
Heterozygosity for two novel n ...... phenotype in a Japanese woman.
@en
Heterozygosity for two novel n ...... phenotype in a Japanese woman.
@nl
type
label
Heterozygosity for two novel n ...... phenotype in a Japanese woman.
@en
Heterozygosity for two novel n ...... phenotype in a Japanese woman.
@nl
prefLabel
Heterozygosity for two novel n ...... phenotype in a Japanese woman.
@en
Heterozygosity for two novel n ...... phenotype in a Japanese woman.
@nl
P2093
P2860
P1476
Heterozygosity for two novel n ...... phenotype in a Japanese woman
@en
P2093
Hiroshi Kimura
Kimitaka Sagawa
Kiyoshi Yasumoto
Makoto Tsuneoka
Mikiko Soejima
Takanori Higashitani
P2860
P304
P356
10.1046/J.1365-2141.2002.03368.X
P407
P50
P577
2002-04-01T00:00:00Z