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References

  1. Pereira JC et al. Prenatal determination of the fetal RhD blood group by multiplex PCR: a 7-year Portuguese experience. Prenat Diagn, 2007. [Citation] [RHeference]
  2. Pereira J et al. Gene symbol: RHD. Disease: Rhesus negative blood group. Hum Genet, 2008. [Citation] [RHeference]
  3. Pereira J et al. Novel human pathological mutations. Gene symbol: RHD. Disease: reduced expression (weak D). Hum Genet, 2009. [Citation] [RHeference]
  4. J. Pereira et al. RHD Null Alleles in the Portuguese Population Transfusion Medicine, 2009. — Abstract — [RHeference]
  5. Pereira JC et al. Novel human pathological mutations. Gene symbol: RHD. Disease: Rhesus negative blood group. Hum Genet, 2009. [Citation] [RHeference]
  6. Pereira JC et al. RhD variant caused by an in-frame triplet duplication in the RHD gene. Transfusion, 2011. [Citation] [RHeference]
  7. Dezan MR et al. RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients. Blood Cells Mol Dis, 2017. [Citation] [RHeference]
  8. Dezan MR et al. Evaluation of the applicability and effectiveness of a molecular strategy for identifying weak D and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD*Ψ. Transfusion, 2018. [Citation] [RHeference]