Associated Papers
A novel RHD allele, RHD*1166delA, with D-negative phenotype identified in a Chinese family.
Zhang X et al.
Transfusion, 2022
Frameshift variations in the RHD coding sequence: Molecular mechanisms permitting protein expression.
Flegel WA et al.
Transfusion, 2020
Molecular and computational analysis of 45 samples with a serologic weak D phenotype detected among 132,479 blood donors in northeast China.
Zhang X et al.
Journal of Translational Medicine, 2019
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