1. Molecular basis of weak D phenotypes;Blood
2. PCR screening for common weak D types shows different distributions in three Central European populations;Transfusion
3. Resolving variable maternal D typing using serology and genotyping in selected prenatal patients;Transfusion
4. Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention;Transfusion