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- 2018
-
Mark
More data needed to establish maternal breast milk IgG as cause for anti-D hemolytic disease of fetus and newborn
(
- Contribution to journal › Letter
-
Mark
FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon
(
- Contribution to journal › Article
-
Mark
Disruption of a GATA-1 binding motif 3.7 KB upstream of the XG/PBDX gene abolishes erythroid Xga expression and elucidates the last unresolved blood group system
2018) 35th international congress of the International Society of Blood Transfusion, ISBT, 2018 In Vox Sanguinis 113(S1). p.62-63(
- Contribution to journal › Published meeting abstract
- 2017
-
Mark
SMIM1 variants rs1175550 and rs143702418 independently modulate Vel blood group antigen expression
(
- Contribution to journal › Article
-
Mark
The Vel blood group system : a review
(
- Contribution to journal › Scientific review
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Mark
Concordance between genotype and blood group phenotype in the INTERVAL cohort of 50,000 English blood donors
(
- Contribution to conference › Abstract
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Mark
The ins and outs of SMIM1 and its relationship to the expression of Vel blood group antigen
2017) 27th Regional Congress of the International Society of Blood Transfusion, ISBT 2017 In Vox Sanguinis 112(Suppl. 1). p.48-49(
- Contribution to journal › Published meeting abstract
-
Mark
A and B antigen levels acquired by group O donor-derived erythrocytes following ABO-non-identical transfusion or minor ABO-incompatible haematopoietic stem cell transplantation
(
- Contribution to journal › Article
- 2016
-
Mark
A novel RHCE*02 allele, containing the single-nucleotide change c.460A>G, encodes weakened expression of C and e antigens
(
- Contribution to journal › Article
-
Mark
Säkerhetslaboratorium underlättar hantering av smittor som ebola.
(
- Contribution to journal › Article