Associated Papers
DEL variants: review of molecular mechanisms, clinical consequences and molecular testing strategy.
Yin Q
Functional & Integrative Genomics, 2023
Functional analysis of novel RHD variants: splicing disruption is likely to be a common mechanism of variant D phenotype.
Raud L et al.
Transfusion, 2019
The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.
Scott SA et al.
Transfusion, 2014
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