Associated Papers
Alloanti-D induction in a rare RhD variant (DBT-2) case: Insights from serological and molecular biological testing.
Xu Z et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2025
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa.
Mbeti JMM et al.
Blood Transfusion = Trasfusione Del Sangue, 2024
Characterization of Novel RHD Allele Variants and Their Implications for Routine Blood Group Diagnostics.
Matzhold EM et al.
Biomedicines, 2024
Transfusion management of Africans with RHD variants in China.
Yin Q et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2023
RHD Genotypes in a Chinese Cohort of Pregnant Women.
Zhang J et al.
Frontiers in Genetics, 2021
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.
Lopez GH et al.
Transfusion, 2016
Distribution of Rhesus blood group antigens and weak D alleles in the population of Albania.
Xhetani M et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
Partial D phenotypes and genotypes in the Chinese population.
Ye L et al.
Transfusion, 2012
Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese.
Shao CP et al.
Vox Sanguinis, 2002
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