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KEL*02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,-2 phenotypes.
Vox Sang. 2010 Aug 1;99(2):150-7. doi: 10.1111/j.1423-0410.2010.01334.x. Epub 2010 Apr 4.
Vox Sang. 2010.
PMID: 20384970
Characterization of Jk(a+(weak)): a new blood group phenotype associated with an altered JK*01 allele.
Wester ES, Storry JR, Olsson ML.
Wester ES, et al.
Transfusion. 2011 Feb;51(2):380-92. doi: 10.1111/j.1537-2995.2010.02795.x.
Transfusion. 2011.
PMID: 21309779
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Phenotype prediction by DNA-based typing of clinically significant blood group systems in Jordanian blood donors.
Irshaid NM, Ramadan S, Wester ES, Olausson P, Hellberg A, Merza JY, Olsson ML.
Irshaid NM, et al. Among authors: wester es.
Vox Sang. 2002 Jul;83(1):55-62. doi: 10.1046/j.1423-0410.2002.00182.x.
Vox Sang. 2002.
PMID: 12100390
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Blood group genotype analysis for the quality improvement of reagent test red blood cells.
Hult A, Hellberg A, Wester ES, Olausson P, Storry JR, Olsson ML.
Hult A, et al. Among authors: wester es.
Vox Sang. 2005 May;88(4):265-70. doi: 10.1111/j.1423-0410.2005.00623.x.
Vox Sang. 2005.
PMID: 15877648
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Genetic basis of the K(0) phenotype in the Swedish population.
Wester ES, Storry JR, Schneider K, Nilsson Sojka B, Poole J, Olsson ML.
Wester ES, et al.
Transfusion. 2005 Apr;45(4):545-9. doi: 10.1111/j.0041-1132.2005.04283.x.
Transfusion. 2005.
PMID: 15819675
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Erythroid urea transporter deficiency due to novel JKnull alleles.
Wester ES, Johnson ST, Copeland T, Malde R, Lee E, Storry JR, Olsson ML.
Wester ES, et al.
Transfusion. 2008 Feb;48(2):365-72. doi: 10.1111/j.1537-2995.2007.01532.x. Epub 2007 Nov 19.
Transfusion. 2008.
PMID: 18028269
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A simple screening assay for the most common JK*0 alleles revealed compound heterozygosity in Jk(a-b-) probands from Guam.
Wester ES, Gustafsson J, Snell B, Spruell P, Hellberg A, Olsson ML, Storry JR.
Wester ES, et al.
Immunohematology. 2009;25(4):165-9.
Immunohematology. 2009.
PMID: 20406024
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