Systematic RHD genotyping in Brazilians reveals a high frequency of partial D in transfused patients serologically typed as weak D
Author:
Funder
Fundação de Amparo à Pesquisa do Estado de São Paulo
Publisher
Elsevier BV
Subject
Hematology
Reference25 articles.
1. Variantes of RhD-current testing and clinical consequences;Daniels;Br J Haematol,2013
2. Molecular genetics and clinical applications for RH;Flegel;Transfus Apher Sci,2011
3. It’s time to phase in RHD genotyping for patients with a serologic weak D phenotype;Sandler;Transfusion,2015
4. On the complexity of D antigen typing: a hand decision tree in the age of molecular blood group diagnostics;Flegel;J Obstet Gynaecol Can,2007
5. Molecular basis of weak D phenotypes;Wagner;Blood,1999
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Implication of novel RH alleles in blood transfusion therapy;Annals of Blood;2023-12
2. RHD genotyping to resolve weak and discrepant RhD patient phenotypes;Transfusion;2022-10-11
3. Dilema de las variantes Rh;Revista Mexicana de Medicina Transfusional;2022
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