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List of works by Eunike C McGowan

A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype

scientific article published on 8 July 2016

A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms.

scientific article

A proposed new low-frequency antigen in the Augustine blood group system associated with a severe case of hemolytic disease of the fetus and newborn.

scientific article published on 5 March 2018

Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management

scientific article published on 20 February 2017

Evaluation of targeted exome sequencing for 28 protein-based blood group systems, including the homologous gene systems, for blood group genotyping

scientific article published on 24 March 2017

Genotyping by sequencing defines independent novel RHD variants for an antenatal patient and a blood donor.

scientific article published on 16 July 2017

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)

scientific article published on 17 September 2018

Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting.

scientific article published on 8 November 2017

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