References
- 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]
- Daniels GL et al. The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis. Transfusion, 1998. [Citation] [RHeference]
- Singleton BK et al. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in africans with the Rh D-negative blood group phenotype. Blood, 2000. [Citation] [RHeference]
- Singleton BK. Green CA et al. Two new RHD mutations associated with the DEL phenotype Transfusion Clinique et Biologique, 2001. — Abstract — [RHeference]
- Körmöczi GF et al. Molecular and serologic characterization of DWI, a novel "high-grade" partial D. Transfusion, 2004. [Citation] [RHeference]
- Green C et al. Evidence that a mutation in a splice site of RHD intron 2 causes alternative splicing of RHD exon 3 Vox Sanguinis, 2011. — Abstract — [RHeference]