Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD‐specific exons
- 12 November 1998
- journal article
- research article
- Published by Wiley in Transfusion
- Vol. 38 (11-12) , 1015-1021
- https://doi.org/10.1046/j.1537-2995.1998.38111299056309.x
Abstract
BACKGROUND: Qualitative RHD variants are the result of the replacement of RHD exons by their RHCE counterparts or of point mutations in RHD causing amino acid substitutions. For RHD typing, the use o...Keywords
This publication has 36 references indexed in Scilit:
- Specificity and sensitivity of RHD genotyping methods by PCR‐based DNA amplificationBritish Journal of Haematology, 1997
- The RHD gene is highly detectable in RhD-negative Japanese donors.Journal of Clinical Investigation, 1997
- Lower antigen site density and weak D immunogenicity cannot be explained by structural genomic abnormalities or regulatory defects of the RHD geneTransfusion, 1997
- Molecular background of VS and weak C expression in blacksTransfusion, 1997
- Characterization of the hybrid RHD gene leading to the partial D category IIIc phenotypeTransfusion, 1996
- The genetic basis of a new partial D antigen: DDBTBritish Journal of Haematology, 1996
- Involvement of Ser103 of the Rh polypeptides in G epitope formationTransfusion, 1996
- Leu110Pro substitution in the RhD polypeptide is responsible for the DVII category blood group phenotypeAmerican Journal of Hematology, 1995
- Serotype Switching in a Partially Deleted RHD GeneVox Sanguinis, 1994
- Prenatal determination of fetal RhD typeThe Lancet, 1994