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
Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden.
Pardi C et al.
Blood Transfusion = Trasfusione Del Sangue, 2024
RHD Genotyping of Rh-Negative and Weak D Phenotype among Blood Donors in Southeast Iran.
Sadeghi-Bojd Y et al.
International Journal of Hematology-oncology and Stem Cell Research, 2021
RHD Genotypes in a Chinese Cohort of Pregnant Women.
Zhang J et al.
Frontiers in Genetics, 2021
RHD genotyping of serological weak D phenotypes in the Iranian blood donors and patients.
Oodi A et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2020
Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele.
Fichou Y et al.
Transfusion, 2018
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
Partial D phenotypes and genotypes in the Chinese population.
Ye L et al.
Transfusion, 2012
Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypes.
Brajovich ME et al.
Transfusion, 2012
RHD(T201R, F223V) cluster analysis in five different ethnic groups and serologic characterization of a new Ethiopian variant DARE, the DIII type 6, and the RHD(F223V).
Grootkerk-Tax MG et al.
Transfusion, 2006
PCR screening for common weak D types shows different distributions in three Central European populations.
Müller TH et al.
Transfusion, 2001
Polymorphisms of RhD(Va) and a new RhD(Va)-like variant found in Japanese individuals.
Hyodo H et al.
Vox Sanguinis, 2000
RHD genotyping in weak D phenotypes by multiple polymerase chain reactions.
Legler TJ et al.
Transfusion, 1998