Blood group molecular genotyping

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kidd blood group genotyping in alloimmunized thallasemia patients

Abstract Background and Objectives Hemagglutination has limitations in identifying the phenotype of patients who have been recently transfused due to the presence of donor red cells (RBCs) in the patient’s circulation. Kidd blood group is one of the most important blood groups in transfusion medicine and related antibodies are responsible for one third of delayed haemolytic transfusion reactio...

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Blood Group ABO Genotyping in Paternity Testing.

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BACKGROUND Duffy (FY) blood group genotyping is important in transfusion medicine because Duffy alloantibodies are associated with delayed hemolytic transfusion reactions and hemolytic disease of the fetus and newborn. In this study, FY allele frequencies in Thai blood donors were determined by in-house PCR with sequence-specific primers (PCR-SSP), and the probability of obtaining compatible bl...

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Report of the third international workshop on molecular blood group genotyping.

The Third International Society of Blood Transfusion Workshop on Molecular Blood Group Genotyping was held in 2008, with a feedback meeting at the International Society of Blood Transfusion Congress in Macao SAR, China. Thirty-three laboratories participated, eight less than in 2006. Six samples were distributed: sample 1 representing DNA from a sample referred because of abnormal serological r...

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Rh blood group genotyping in alloimmunized thalassemic patientsin Tehran Adult Thalassemia Clinic during 2017-18

Abstract Background and Objectives The main antigens of the Rh blood group system (D,C,c,E,e) after the ABO system, are the most immune antigens. Due to existence of donor's red blood cells in the patient's circulation serologic methods can not accurately detect blood group antigens in patients with chronic blood transfusions, but molecular methods can overcome many of these limitations.   ...

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ژورنال

عنوان ژورنال: ISBT Science Series

سال: 2011

ISSN: 1751-2816

DOI: 10.1111/j.1751-2824.2011.01523.x