RHeference
  • Allele
    • List
    • Search
  • References
    • All
    • By Author
    • By Journal
  • Documentation
  • Statistics
  • Search
    • By name
    • By mutation
    • In exons
    • Complex
  • Contact

References

  1. Feng J et al. A new RHD variant allele is caused by a RHD 662C>G mutation. Transfusion, 2017. [Citation] [RHeference]
  2. Liao Z et al. [A weak D type 59 case identified in the Chinese Han population]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2018. [Citation] [RHeference]
  3. Zhu Y et al. A new RHD variant allele in Exon 2 identified in a Chinese individual. Transfusion, 2019. [Citation] [RHeference]