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红细胞血型相关

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 RHCE*03 with 255G > A, 538G > A, and Exon 9 of RHD in a Chinese individual encodes for altered c and E antigens

Detecting serologically difficult ABO blood groups using single-molecule real-time sequencing technology

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 Research of a Large-Scale Analysis Platform for MNS Blood Group Identification Based on Long-Read Sequencing

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

Third-Generation Sequencing Reveals an ABO Gene Promoter Mutation, Leading to Weakened B Antigen Expression

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

Comprehensive Annotation of Complete ABO Alleles and Resolution of ABO Variants by an Improved Full-Length ABO Haplotype Sequencing

PacBio third-generation sequencing detects a new variant, c.27delC, in exon 1 of the ABO gene resulting in a weak B phenotype

Identification of a novel variant (c.1-111A>G) located in GATA-1 motif of RHCE proximal promoter in two Chinese patients with the rare D-- phenotype

A case report of a rare p phenotype individual and a review of molecular biological analysis of p phenotype in the Chinese population

1例RHD⁃CE(3⁃7)⁃D 基因重组与RHCE变异型患者的血清学与分子生物学分析

A novel RHCE*02 variant with a recombination of RHD exon 3 in a Chinese D+ voluntary blood donor with weak expression of e antigen




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