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Article

Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD*148+1T (RHD*01EL.31). Turley E, McGowan EC, Hyland CA, Schoeman EM, Flower RL, Skoll A, Delisle MF, Nelson T, Clarke G, Au N. Transfusion, 2018. [Citation]

Annotations by Allele

  • RHD*148+1T (IVS1+1T, DEL31): RH1 (adsorption-elution was performed)
  • RHD*148+1T (IVS1+1T, DEL31): Serology
  • RHD*148+1T (IVS1+1T, DEL31): otherHaplotype (related samples)
  • RHD*148+1T (IVS1+1T, DEL31): AbSpecificity
  • RHD*148+1T (IVS1+1T, DEL31): Prevalence