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- 2022
-
Mark
A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B
w phenotype.
(
- Contribution to journal › Article
- 2018
-
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
- 2017
-
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
- 2015
-
Mark
An Age-dependent ABO Discrepancy Between Mother And Baby Reveals A Novel Aweak Allele
(
- Contribution to journal › Article
-
Mark
Identification of the molecular and genetic basis of PX2, a glycosphingolipid blood group antigen lacking on globoside-deficient erythrocytes.
(
- Contribution to journal › Article
-
Mark
RIFINs are adhesins implicated in severe Plasmodium falciparum malaria.
(
- Contribution to journal › Article
- 2013
-
Mark
Forssman expression on human erythrocytes: biochemical and genetic evidence of a new histo-blood group system
(
- Contribution to journal › Article
- 2010
-
Mark
Discrepant Serologic Abo Typing In An Unusual Para-Bombay Ab(H) Sample Caused By Compound Heterozygosity For Different Fut1 Mutations
(
- Contribution to journal › Published meeting abstract
-
Mark
Novel Non-Deletional O Alleles Based on A or B Sequences Give Rise to Erroneous ABO Genotyping Results
(
- Contribution to journal › Published meeting abstract
- 2005
-
Mark
Blood group genotype analysis for the quality improvement of reagent test red blood cells
(
- Contribution to journal › Article