The complexity of the RHD and RHCE genes, which is the greatest of all bloo
d group systems, confounds analysis at the molecular level. RH DNA typing w
as introduced in 1993 and has been applied to prenatal testing. PCR-SSP ana
lysis covering multiple polymorphisms was recently introduced for the scree
ning and initial characterization of partial D. Our objective is to summari
ze the accrued knowledge relevant to the approaches to Rh phenotype predict
ion by DNA typing, their possible applications beyond research laboratories
and their limitations. The procedures, results and problems encountered ar
e highly detailed. It is recommended that DNA typing comprises an analysis
of more than one polymorphism. We discuss future directions and propose a p
iecemeal approach to improve reliability and cost-efficiency of blood group
genotyping that may eventually replace the prevalent serology-based techni
ques even for many routine tasks. Transfusion medicine is in the unique pos
ition of being able to utilize the most extensive phenotype databases avail
able to check and develop genotyping strategies.