References

1. Li Q et al. [Study on the molecular background of Del phenotype in Chinese population]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2006. [Citation] [RHeference]
2. Ye LY et al. Molecular and family analyses revealed two novel RHD alleles in a survey of a Chinese RhD-negative population. Vox Sang, 2007. [Citation] [RHeference]
3. Li Q et al. Molecular basis of D variants between Uigur and Han blood donors in Xinjiang. Transfus Med, 2008. [Citation] [RHeference]
4. Li Q et al. Molecular basis of the RHD gene in blood donors with DEL phenotypes in Shanghai. Vox Sang, 2009. [Citation] [RHeference]
5. Ye L et al. Molecular bases of unexpressed RHD alleles in Chinese D- persons. Transfusion, 2009. [Citation] [RHeference]
6. Ye L et al. Partial D phenotypes and genotypes in the Chinese population. Transfusion, 2012. [Citation] [RHeference]
7. Ye L et al. Weak D phenotypes caused by intronic mutations in the RHD gene: four novel weak D alleles identified in the Chinese population. Transfusion, 2013. [Citation] [RHeference]
8. Zhang J et al. Identification of a novel missense mutation (p.Ser230Asn) in RHD allele in a Chinese individual with partial D phenotype. Transfusion, 2018. [Citation] [RHeference]
9. He Y et al. [A case with a novel weak D type]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2019. [Citation] [RHeference]