Associated Papers
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
Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
Chang TC et al.
Blood Advances, 2024
38522094 (PubMed )
Supplement: BLOODA_ADV-2023-011660-mmc1.xlsx › Rh__2_
Classification of major and minor blood group antigens in the Kuwaiti Arab population.
Ameen R et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2020
RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients.
Dezan MR et al.
Blood Cells, Molecules & Diseases, 2017
Identification of six new RHCE variant alleles in individuals of diverse racial origin.
Goldman M et al.
Transfusion, 2016
Molecular structures identified in serologically D- samples of an admixed population.
Trucco Boggione C et al.
Transfusion, 2014
RHD*weak partial 4.0 is associated with an altered RHCE*ce(48C, 105T, 733G, 744C, 1025T) allele in the Tunisian population.
Ouchari M et al.
Transfusion Medicine (oxford, England), 2013
Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease.
Pham BN et al.
Transfusion, 2011
RhCE protein variants in Southwestern Germany detected by serologic routine testing.
Bugert P et al.
Transfusion, 2009
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