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- 2020
- May the FORS be with you : a system sequel (
- A novel ABO allele with a 21-bp duplication identified in two unrelated European individuals with weak A expression (
- 2019
- Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus (
- A novel single-nucleotide substitution in the proximal ABO promoter gives rise to the B3 phenotype (
- Synthesis of blood group Forssman pentasaccharide GalNAcα1-3GalNAcβ1-3Galα1-4Galβ1-4Glcβ–R (
- 2018
- FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon (
- GBGT1 is allelically diverse but dispensable in humans and naturally occurring anti-FORS1 shows an ABO-restricted pattern (
- GBGT1 is allelically diverse but dispensible in humans and naturally-occurring anti-FORS1 shows an ABO-restricted pattern (
- 2017
- 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 (
- The FORS awakens : Review of a blood group system reborne (