References
- Liu et al. Molecular analysis of two D-variants, DHMi and DHMii. Transfusion Medicine, 1996. — Abstract — [RHeference]
- Scott M et al. Rh serology--coordinator's report. Transfus Clin Biol, 1996. [Citation] [RHeference]
- Scott ML et al. A structural model for 30 Rh D epitopes based on serological and DNA sequence data from partial D phenotypes. Transfus Clin Biol, 1996. [Citation] [RHeference]
- Avent ND et al. Molecular biology of partial D phenotypes. Transfus Clin Biol, 1996. [Citation] [RHeference]
- Wallace M et al. DBT: a partial D phenotype associated with the low-incidence antigen Rh32. Transfus Med, 1997. [Citation] [RHeference]
- Jones JW et al. The serological profile and molecular basis of a new partial D phenotype, DHR. Vox Sang, 1997. [Citation] [RHeference]
- Avent ND et al. Molecular basis of the D variant phenotypes DNU and DII allows localization of critical amino acids required for expression of Rh D epitopes epD3, 4 and 9 to the sixth external domain of the Rh D protein. Br J Haematol, 1997. [Citation] [RHeference]
- Avent ND et al. Molecular analysis of Rh transcripts and polypeptides from individuals expressing the DVI variant phenotype: an RHD gene deletion event does not generate All DVIccEe phenotypes. Blood, 1997. [Citation] [RHeference]
- Liu W et al. Site-directed mutagenesis of the human D antigen: definition of D epitopes on the sixth external domain of the D protein expressed on K562 cells. Transfusion, 1999. [Citation] [RHeference]
- Scott SA et al. The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes. Transfusion, 2014. [Citation] [RHeference]
- Lopez GH et al. A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms. Transfusion, 2018. [Citation] [RHeference]