46 – 60 of 234
- show: 15
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2020
-
Mark
Association of Maternal Regulatory Single Nucleotide Polymorphic CD99 Genotype with Preeclampsia in Pregnancies Carrying Male Fetuses in Ethiopian Women
(
- Contribution to journal › Article
-
Mark
External quality assessment of noninvasive fetal RHD genotyping
(
- Contribution to journal › Article
-
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
-
Mark
Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype
(
- Contribution to journal › Article
-
Mark
The Xg blood group system : no longer forgotten
(
- Contribution to journal › Letter
-
Mark
May the FORS be with you : a system sequel
(
- Contribution to journal › Scientific review
-
Mark
SMIM1, carrier of the Vel blood group, is a tail-anchored transmembrane protein and readily forms homodimers in a cell-free system
(
- Contribution to journal › Article
-
Mark
A novel ABO allele with a 21-bp duplication identified in two unrelated European individuals with weak A expression
(
- Contribution to journal › Article
-
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
-
Mark
ABO and Other Carbohydrate Blood Group Systems
2020) p.816-816(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Akademiskt hushållsarbete. Kan vi hjälpas åt att synliggöra det?
2020)(
- Book/Report › Report
-
Mark
The P1PK blood group system : revisited and resolved
(
- Contribution to journal › Article
- 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
-
Mark
Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus
(
- Contribution to journal › Article
-
Mark
The P1 histo-blood group antigen is present on human red blood cell glycoproteins
(
- Contribution to journal › Article