A novel ABO allele with a 21‐bp duplication identified in two unrelated European individuals with weak A expression
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DOI: 10.1111/tme.12730
Abstract: To carry out genetic and serological analyses of a Swiss blood donor and a Danish patient carrying an aberrant ABO phenotype with weak A expression. read more here.
Keywords: weak expression; abo allele; abo; allele duplication ... See more keywords
c.125_126insT mutation in ABO*B.01 allele responsible for Bel phenotype
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DOI: 10.1111/trf.14928
Abstract: Red blood cell (RBC) phenotypes of the proband and his family members were determined using routine serologic techniques. Briefly, the RBCs of these individuals were reacted with anti-A, anti-B, anti-AB (Shanghai HemoPharmaceutical Biological Company), and… read more here.
Keywords: mutation abo; abo allele; responsible bel; 125 126inst ... See more keywords
c.586T>C mutation on the ABO*A1.02 allele responsible for Ael phenotype
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DOI: 10.1111/trf.16890
Abstract: ABO subgroups result from ABO gene variants which brings about the ABO typing discrepancy. ABO*A1.01 allele is used as a reference for the sequences of all other ABO alleles. Many of the A suballeles contain… read more here.
Keywords: 586t mutation; abo; ael phenotype; abo allele ... See more keywords
Identification of a novel A allele with a c.977A>C variation on the ABO*A1.02 allele
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DOI: 10.1111/trf.17051
Abstract: The ABO blood group system was the first human blood group to be discovered and is of great signifi-cance in transfusion medicine. Currently, it needs to perform compatibility for ABO blood group in clinical blood… read more here.
Keywords: abo allele; abo; variation; blood group ... See more keywords
Identification of a novel ABO*A1.02 allele with variant c.671T>C
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DOI: 10.1111/trf.17206
Abstract: As the first discovered blood group system, the ABO blood group plays a critical role in blood transfusion and hemolytic disease in newborns. Subgroup phenotypes, such as A2, Aint, A3, cisAB, B3, and Bel, have… read more here.
Keywords: novel abo; variant 671t; blood; abo allele ... See more keywords
c.5del mutation on the ABO*B.01 allele responsible for Bx phenotype
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DOI: 10.1111/trf.17231
Abstract: Five samples from the proband and her four familial members were analyzed. This study was approved by the Ethics Review Committee of the Department of Blood Transfusion, Shengjing Hospital of China Medical University (approval no.:… read more here.
Keywords: allele responsible; abo allele; mutation abo; responsible phenotype ... See more keywords
Identification of a novel A allele with a c.102C > A variation on the ABO*A1.02 allele
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DOI: 10.1111/trf.17257
Abstract: Identifying ABO blood group correctly is of great significance to ensure safety of clinical blood transfusion. The ABO blood group system is one of the important blood group systems in clinical blood transfusion. ABO variant… read more here.
Keywords: allele 102c; abo; blood group; blood ... See more keywords