Novel missense mutation c.797TC gives rise to the rare B(A) phenotype in a Chinese family
Detection and phenotype analysis of a novel Ael blood group allele
Identification of a novel O allele with c.777C>G on an ABO*O.01.02 background
A novel c.29‐3C>G variant on the B allele forms the Bel phenotype
Integrated analyses reveal unexpected complex inversion and recombination in RH genes
A novel FUT1*932A allele associated with the para‐Bombay A phenotype in a Chinese individual
The Novel Variant c.122delG on the ABO*B3.0x Allele Associated with B3 Phenotype
Identification of a novel c.506A>C variant on the ABO*A1.02 allele in a Chinese individual
Identification of an AweakB phenotype caused by significant ABO gene deletion
Identification of a novel RHAG allele with a c.500A>G variation associated with Rhmod phenotype
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