Abstract
This reference was identified in a congress abstract or in an online resource.
Severe case of haemolytic disease of fetus and newborn occurring in baby who has inherited a novel RHD allele associated with a “partial” RhD positive phenotype . J Morrison, R Turner, G Millard, G Lopez, S Williams, T Powley, Y Liew, R Flower and C Hyland. Vox Sanguinis, 2019.
Remark: vol. 114 (S1), pp. 205.0, abstract P-445
Annotations by Allele
- RHD*DIII-CE(9)-D(604A): RH1
- RHD*DIII-CE(9)-D(604A): RH
- RHD*DIII-CE(9)-D(604A): RH
- RHD*DIII-CE(9)-D(604A): otherHaplotype
- RHD*DIII-CE(9)-D(604A): Prevalence