Associated Papers
Forward and reverse genomic screens enhance the understanding of phenotypic variation in a large Chinese rhesus macaque cohort.
Zhang BL et al.
Nature Communications, 2025
41027928 (PubMed )
Supplement: 41467_2025_63747_MOESM4_ESM.xlsx › Supplementary_Data_2
Molecular characterization of rare D--/D-- variants in individuals of Indian origin.
Kulkarni S et al.
Blood Transfusion = Trasfusione Del Sangue, 2022
D--phenotype due to RHD-RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti-Rh 17(Hrₒ) antibodies.
Mani A et al.
Transfusion Medicine (oxford, England), 2021
Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms.
Chen JM et al.
Transfusion, 2013
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