Associated Papers
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
Genomic characterization of the RH locus detects complex and novel structural variation in multi-ethnic cohorts.
Wheeler MM et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
29955105 (PubMed )
Supplement: NIHMS969264-supplement-Supplementary___Appendix__online_only_material__etc__.pdf
New RHCE variant alleles encoding the D- - phenotype.
Ochoa-Garay G et al.
Transfusion, 2013
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