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- 2009
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Mark
A simple screening assay for the most common JK*0 alleles revealed compound heterozygosity in Jk(a-b-) probands from Guam
(
- Contribution to journal › Article
- 2008
-
Mark
Flow cytometric evaluation of red blood cells transformed with variable amounts of synthetic A and B glycolipids
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.180-180(
- Contribution to journal › Published meeting abstract
-
Mark
Pre-transplantation confirmatory ABO genotyping reveals a novel non-deletional 0 allele
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.178-178(
- Contribution to journal › Published meeting abstract
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Mark
Erythroid urea transporter deficiency due to novel JK(null) alleles
(
- Contribution to journal › Article
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Mark
ABO transcript levels in peripheral blood and erythropoietic culture show different allele-related patterns independent of the CBF/NF-Y enhancer motif and multiple novel allele-specific variations in the 5'- and 3'-noncoding regions.
(
- Contribution to journal › Article
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Mark
Investigation into A antigen expression on O-2 heterozygous group O-labeled red blood cell units
(
- Contribution to journal › Article
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Mark
Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotype.
(
- Contribution to journal › Article
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Mark
Serologic and molecular characterization of an ab individual with dual expression of a antigen - A case report
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.199-200(
- Contribution to journal › Published meeting abstract
-
Mark
Molecular analysis of DNA from Danish blood donors revealed a novel allele with a mutation in exon 8 resulting in a very weak K phenotype
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.200-201(
- Contribution to journal › Published meeting abstract
-
Mark
Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles
(
- Contribution to journal › Article