RHeference
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References

  1. Gorick B et al. Quantitation of D sites on selected 'weak D' and 'partial D' red cells. Vox Sang, 1993. [Citation] [RHeference]
  2. Simsek S et al. Rapid Rh D genotyping by polymerase chain reaction-based amplification of DNA. Blood, 1995. [Citation] [RHeference]
  3. Beckers EA et al. The R0Har RH:33 phenotype results from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene. Br J Haematol, 1996. [Citation] [RHeference]
  4. Hazenberg CA et al. Hemolytic disease of the newborn caused by alloanti-D from an R0Har r Rh:33 mother. Transfusion, 1996. [Citation] [RHeference]
  5. Beckers EA et al. The RoHar antigenic complex is associated with a limited number of D epitopes and alloanti-D production: a study of three unrelated persons and their families. Transfusion, 1996. [Citation] [RHeference]
  6. Faas BH et al. Involvement of Ser103 of the Rh polypeptides in G epitope formation. Transfusion, 1996. [Citation] [RHeference]
  7. Beckers EA et al. The genetic basis of a new partial D antigen: DDBT. Br J Haematol, 1996. [Citation] [RHeference]
  8. Beckers EA et al. Characterization of the hybrid RHD gene leading to the partial D category IIIc phenotype. Transfusion, 1996. [Citation] [RHeference]
  9. Faas BH et al. Molecular background of VS and weak C expression in blacks. Transfusion, 1997. [Citation] [RHeference]
  10. Wallace M et al. DBT: a partial D phenotype associated with the low-incidence antigen Rh32. Transfus Med, 1997. [Citation] [RHeference]
  11. Maaskant-van Wijk PA et al. Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons. Transfusion, 1998. [Citation] [RHeference]