References

  1. Nogues N et al. RHD null alleles in the Spanish population Vox Sanguinis, 2007. — Abstract — [RHeference]
  2. MP Martinez Badas et al. Anti-D immunization in a D-positive mother Vox Sanguinis, 2007. — Abstract — [RHeference]
  3. M Rodrigues et al. A novel RHD variant 'DFW-2' Vox Sanguinis, 2009. — Abstract — [RHeference]
  4. Green C et al. Evidence that a mutation in a splice site of RHD intron 2 causes alternative splicing of RHD exon 3 Vox Sanguinis, 2011. — Abstract — [RHeference]
  5. St-Louis R et al. DEL Blood donors alloimmunised patients: the Canadian experience Vox Sanguinis, 2012. — Abstract — [RHeference]
  6. Wagner FF et al. RHD PCR of blood donors in Northern Germany: use of adsorption/elution to determine D antigen status Vox Sanguinis, 2012. — Abstract — [RHeference]
  7. Duran JA et al. New RHD variant found in Portuguese blood donors Vox Sanguinis, 2012. — Abstract — [RHeference]
  8. Horn T et al. RHD*DIII.4 allele with additional nucleotide change 307 T>C Vox Sanguinis, 2012. — Abstract — [RHeference]
  9. Villa MA et al. A novel mutation of the RHD antigen Vox Sanguinis, 2012. — Abstract — [RHeference]
  10. Quaglietta A et al. Case-report of a newly described RHD allele Vox Sanguinis, 2015. — Abstract — [RHeference]
  11. Moser I et al. A novel RHD allele resulting in a weak D variant Vox Sanguinis, 2015. — Abstract — [RHeference]
  12. Lambert MD et al. The second example of alloanti-D in a weak D type 33 individual Vox Sanguinis, 2015. — Abstract — [RHeference]
  13. C Henny et al. Impact of the mandatory donor RHD screening in Switzerland Vox Sanguinis, 2016. — Abstract — [RHeference]
  14. A Matteocci et al. Identification of weak D type 100 in two unrelated italian donors Vox Sanguinis, 2017. — Abstract — [RHeference]
  15. M Pisacka et al. Two novel partial D antigens, characterized by single missense nontemplated mutations causing a significant impact on RHD protein tertial structure and d epitopes expression Vox Sanguinis, 2018. — Abstract — [RHeference]
  16. J Morrison et al. Severe case of haemolytic disease of fetus and newborn occurring in baby who has inherited a novel RHD allele associated with a “partial” RhD positive phenotype Vox Sanguinis, 2019. — Abstract — [RHeference]
  17. L Castilho et al. From genotyping to the functional and clinical interpretation of variations in blood group genes by 3D-protein structure investigation: two novel variant alleles in the RHD gene Vox Sanguinis, 2019. — Abstract — [RHeference]
  18. C von Arx et al. A novel RHD splice donor site mutation leading to a RhD-negative phenotype Vox Sanguinis, 2019. — Abstract — [RHeference]
  19. CS Principi et al. Genetic characterization of the RH haplotype in individuals carrying the RHD*46C DEL allele Vox Sanguinis, 2019. — Abstract — [RHeference]
  20. GA Denomme et al. A novel weak D 4.0-related allele and RHCE*ceCF defines a new rh haplotype in an autologous donor with an antibody to a high frequency antigen Vox Sanguinis, 2019. — Abstract — [RHeference]
  21. L Castilho et al. RHD*weak D type 3 and production of allo-anti-D in a patient with sickle cell disease (SCD)
 Vox Sanguinis, 2019. — Abstract — [RHeference]
  22. M Pisacka et al. Strong pregnancy induced anti-D immunization in del phenotype with RHD*01EL.04 allele Vox Sanguinis, 2019. — Abstract — [RHeference]