Detalhe da pesquisa
1.
A cold case of hemolytic disease of the fetus and newborn resolved by genomic sequencing and population studies to define a new antigen in the Rh system.
Transfusion
; 64(6): 1171-1176, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38686705
2.
Hemolytic disease of the fetus and newborn caused by anti-sD antibody in a GP.Mur/Mur Thai mother and review of the prevalence of sD in Thai blood donors.
Transfusion
; 62(10): 2137-2142, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36062546
3.
Fatal haemolytic transfusion reaction due to anti-Ena and identification of a novel GYPA c.295delG variant in a Thai family.
Vox Sang
; 117(11): 1327-1331, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36102166
4.
A new high-prevalence LW antigen detected by an antibody in an Indigenous Australian homozygous for LW*A c.309C>A variant.
Vox Sang
; 117(7): 958-965, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35412682
5.
Frequency of Mia (MNS7) and Classification of Mia-Positive Hybrid Glycophorins in an Australian Blood Donor Population.
Transfus Med Hemother
; 47(4): 279-286, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32884500
6.
Investigation of the variable In(Lu) phenotype caused by KLF1 variants.
Transfusion
; 58(10): 2414-2420, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30222867
7.
A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms.
Transfusion
; 58(3): 685-691, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29214630
8.
Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting.
Transfusion
; 58(2): 284-293, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29119571
9.
Evaluation of targeted exome sequencing for 28 protein-based blood group systems, including the homologous gene systems, for blood group genotyping.
Transfusion
; 57(4): 1078-1088, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28338218
10.
A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.
Transfusion
; 56(9): 2322-30, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27390888
11.
Modified expression of the KEL2 (k) blood group antigen attributed to p.Leu196Val amino acid change three residues from the K/k antigen polymorphism site: implications for donor screening.
Transfusion
; 59(3): 1156-1158, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30586164
12.
A proposed new low-frequency antigen in the Augustine blood group system associated with a severe case of hemolytic disease of the fetus and newborn.
Transfusion
; 58(5): 1320-1322, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29504136
13.
Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor.
Transfusion
; 57(9): 2281-2283, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28714065
14.
Non-invasive fetal RHD genotyping for RhD negative women stratified into RHD gene deletion or variant groups: comparative accuracy using two blood collection tube types.
Pathology
; 49(7): 757-764, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29096879