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References

  1. Chang JG et al. Human RhDel is caused by a deletion of 1,013 bp between introns 8 and 9 including exon 9 of RHD gene. Blood, 1998. [Citation] [RHeference]
  2. Peng CT et al. Molecular basis for the RhD negative phenotype in Chinese. Int J Mol Med, 2003. [Citation] [RHeference]
  3. Hua X et al. A new RHD-positive, D antigen negative allele in Chinese. Vox Sang, 2010. [Citation] [RHeference]
  4. Liu HC et al. Aberrant RNA splicing in RHD 7-9 exons of DEL individuals in Taiwan: a mechanism study. Biochim Biophys Acta, 2010. [Citation] [RHeference]
  5. Wang M et al. Anti-D alloimmunisation in pregnant women with DEL phenotype in China. Transfus Med, 2015. [Citation] [RHeference]
  6. Chen DP et al. Comprehensive analysis of RHD splicing transcripts reveals the molecular basis for the weak anti-D reactivity of Del -red blood cells. Transfus Med, 2016. [Citation] [RHeference]
  7. Feng J et al. A new RHD variant allele is caused by a RHD 662C>G mutation. Transfusion, 2017. [Citation] [RHeference]
  8. 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]
  9. Zhu Y et al. A new RHD variant allele in Exon 2 identified in a Chinese individual. Transfusion, 2019. [Citation] [RHeference]
  10. He Y et al. [A case with a novel weak D type]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2019. [Citation] [RHeference]
  11. Deng D et al. Identification of a novel c.94dupA mutation in RHD allele. Transfusion, 2020. [Citation] [RHeference]