Molecular bases of unexpressedRHDalleles in Chinese D− persons
Author:
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1537-2995.2009.02181.x/fullpdf
Reference14 articles.
1. RHD gene deletion occurred in the rhesus box;Wagner;Blood,2000
2. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype;Singleton;Blood,2000
3. Molecular background of Rh D-positive, D-negative, Del and weak D phenotypes in Chinese;Shao;Vox Sang,2002
4. Systemic analysis and zygosity determination of the RHD gene in a D-negative Chinese Han population reveals a novel D-negative RHD gene;Xu;Vox Sang,2005
5. Molecular basis for the RhD negative phenotype in Chinese;Peng;Int J Mol Med,2003
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2. Polymorphisms in the promoter regions of RHD and RHCE genes in the Chinese Han population;Vox Sanguinis;2023-10-12
3. Noninvasive screening of fetal RHD genotype in Chinese pregnant women with serologic RhD‐negative phenotype;Transfusion;2023-09-12
4. A novel pyrosequencing strategy for RHD zygosity for predicting risk of hemolytic disease of the fetus and newborn;Laboratory Medicine;2023-06-12
5. Transfusion management of Africans with RHD variants in China;Transfusion Clinique et Biologique;2023-05
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