Bahram Hosseini-Maaf
1 – 16 of 16
- show: 50
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2019
-
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
- 2014
-
Mark
Mixed field reactions in ABO and Rh typing chimerism likely resulting from twin haematopoiesis.
(
- Contribution to journal › Article
- 2012
-
Mark
A novel B(weak) hybrid allele lacks three enhancer repeats but generates normal ABO transcript levels.
(
- Contribution to journal › Article
- 2010
-
Mark
A Novel B-Weak Hybrid Allele With A Non-Repeating Cbf-Enhancer Region
(
- Contribution to journal › Published meeting abstract
-
Mark
Increased levels of cell-free hemoglobin, oxidation markers, and the antioxidative heme scavenger alpha(1)-microglobulin in preeclampsia.
(
- Contribution to journal › Article
- 2008
-
Mark
Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles
(
- Contribution to journal › Article
-
Mark
Pre-transplantation confirmatory ABO genotyping reveals a novel non-deletional 0 allele
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.178-178(
- Contribution to journal › Published meeting abstract
-
Mark
Investigation into A antigen expression on O-2 heterozygous group O-labeled red blood cell units
(
- Contribution to journal › Article
- 2007
-
Mark
Structural effects of naturally occurring human blood group B galactosyltransferase mutations adjacent to the DXD motif
(
- Contribution to journal › Article
-
Mark
An extensive polymerase chain reaction-allele-specific polymorphism strategy for clinical ABO blood group genotyping that avoids potential errors caused by null, subgroup, and hybrid alleles
(
- Contribution to journal › Article
-
Mark
Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferase.
(
- Contribution to journal › Article
-
Mark
Genetic Characterisation of Human ABO Blood Group Variants with a Focus on Subgroups and Hybrid Alleles
(
- Thesis › Doctoral thesis (compilation)
- 2005
-
Mark
The A phenotype in the ABO blood group system is due to a splice-site mutation in a hybrid between a new O-like allelic lineage and the A allele.
(
- Contribution to journal › Article
-
Mark
New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes.
(
- Contribution to journal › Article
- 2003
-
Mark
ABO exon and intron analysis in individuals with the A(weak)B phenotype reveals a novel O-1v-A(2) hybrid allele that causes four missense mutations in the A transferase
(
- Contribution to journal › Article
- 2001
-
Mark
Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles
(
- Contribution to journal › Article