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Lista de obras de Elizna M Schoeman

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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.

artículo científico publicado en 2018

Clinically proven mtDNA mutations are not common in those with chronic fatigue syndrome.

artículo científico publicado en 2017

Comprehensive blood group antigen profile predictions for Western Desert Indigenous Australians from whole exome sequence data

scientific article published on 06 December 2018

Developments beyond blood group serology in the genomics era

artículo científico publicado en 2019

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

artículo científico publicado en 2017

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

artículo científico publicado en 2017

Investigation of the variable In(Lu) phenotype caused by KLF1 variants

artículo científico publicado en 2018

Non-invasive fetal RHD genotyping for RhD negative women stratified into RHD gene deletion or variant groups: comparative accuracy using two blood collection tube types.

artículo científico publicado en 2017

Non-invasive prenatal testing (NIPT) for fetal Kell, Duffy and Rh blood group antigen prediction in alloimmunised pregnant women: power of droplet digital PCR

artículo científico publicado en 2020

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.

artículo científico publicado en 2017

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