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- 2020
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Mark
Association of Maternal Regulatory Single Nucleotide Polymorphic CD99 Genotype with Preeclampsia in Pregnancies Carrying Male Fetuses in Ethiopian Women
(
- Contribution to journal › Article
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Mark
Characterization of GYP*Mur and novel GYP*Bun-like hybrids in Thai blood donors reveals a qualitatively altered s antigen
(
- Contribution to journal › Article
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Mark
Gene editing of CD34+ progenitor cells from single blood donor waste bags to create cultured early erythroid cells for study of blood group knock-outs
2020) The 36th International ISBT Congress, Virtual meeting In Vox Sanguinis 115(Suppl. s1). p.363-363(
- Contribution to journal › Published meeting abstract
- 2019
-
Mark
A large deletion spanning XG and GYG2 constitutes a genetic basis of the Xgnull phenotype, underlying anti-Xga production
(
- Contribution to journal › Article
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Mark
International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology : Report of the Dubai, Copenhagen and Toronto meetings
(
- Contribution to journal › Article
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Mark
Automatic for the people : a rapidly evolving movement for the future of genotyping
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- Contribution to journal › Debate/Note/Editorial
- 2018
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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
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Mark
ABO zygosity, but not secretor or Fc receptor status, is a significant risk factor for IVIG-Associated hemolysis
(
- Contribution to journal › Letter
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Mark
Disruption of a GATA1-binding motif upstream of XG/PBDX abolishes Xga expression and resolves the Xg blood group system
(
- Contribution to journal › Article
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Mark
International Forum on typing and matching strategies in patients on anti-CD38 monoclonal therapy
(
- Contribution to journal › Article