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References

  1. Brajovich ME et al. Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypes. Transfusion, 2012. [Citation] [RHeference]
  2. Trucco Boggione C et al. Molecular structures identified in serologically D- samples of an admixed population. Transfusion, 2014. [Citation] [RHeference]
  3. Trucco Boggione C et al. Weak D antigen expression caused by a novel RHD allele in Argentineans. Transfusion, 2016. [Citation] [RHeference]
  4. Boggione CT et al. Genotyping approach for non-invasive foetal RHD detection in an admixed population. Blood Transfus, 2017. [Citation] [RHeference]
  5. CS Principi et al. Genetic characterization of the RH haplotype in individuals carrying the RHD*46C DEL allele Vox Sanguinis, 2019. — Abstract — [RHeference]
  6. Trucco Boggione C et al. Characterization of RHD locus polymorphism in D negative and D variant donors from Northwestern Argentina. Transfusion, 2019. [Citation] [RHeference]
  7. Mufarrege N et al. The novel RHD c.325A>G single nucleotide variation found in Argentineans leads to a partial D phenotype. Transfusion, 2020. [Citation] [RHeference]