Associated Papers
FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon.
Michalewska B et al.
Blood Transfusion = Trasfusione Del Sangue, 2018
Whole exome sequencing in thrombophilic pedigrees to identify genetic risk factors for venous thromboembolism.
Cunha MLR et al.
Plos One, 2017
29117201 (PubMed )
Supplement: pone.0187699.s002.xlsx › SNPs_result_filter_strategies
Genotyping of the rare Para-Bombay blood group in southern Thailand.
Rattanapan Y et al.
Hematology, Transfusion and Cell Therapy, 0
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