References

Chen, D.P., C.F. Sun, H.C. Ning, W.T. Wang and C.P. Tseng, 2016. Comprehensive analysis of RHD splicing transcripts reveals the molecular basis for the weak anti‐D reactivity of Del‐red blood cells. Transfusion Med., 26: 123-129.
CrossRef  |  PubMed  |  Direct Link  |  

Chen, Q., M. Li, X.S. Lu, R. Lu and J. Sun et al., 2012. Molecular basis of weak D and DEL in Han population in Anhui Province, China. Chin. Med. J., 125: 3251-3255.
PubMed  |  Direct Link  |  

Cruz, B.R., A.K. Chiba, E. Moritz and J.O. Bordin, 2012. RHD alleles in Brazilian blood donors with weak D or D‐negative phenotypes. Transfusion Med., 22: 84-89.
CrossRef  |  Direct Link  |  

Flegel, W.A., 2011. Molecular genetics and clinical applications for RH. Transfus. Apher. Sci., 44: 81-91.
CrossRef  |  PubMed  |  Direct Link  |  

Gupta, A., S. Mirza, S. Khurana, R. Singh and S. Chaturvedi et al., 2016. Enigmatic weak D antigen: An experience in a tertiary care hospital of East Delhi. J. Clin. Diagn. Res., 10: EC12-EC15.
PubMed  |  

He, J., Y. Ying, X. Hong, X. Xu, F. Zhu and H. Lv, 2015. Molecular basis and zygosity determination of D variants including identification of four novel alleles in Chinese individuals. Transfusion, 55: 138-143.
CrossRef  |  PubMed  |  Direct Link  |  

ISBT., 2016. Red cell Immunogenetics and blood group terminology. Maharana Pratap Inter State Bus Terminus, Delhi, India. http://www.isbtweb.org/working-parties/red-cell-immunogenetics-and-blood-group-terminology/

Kyaw, T.Z., J.A. Maniam, V.S. Nadarajan and H. Shanmugam, 2012. Molecular analysis of Malaysian Chinese D-donors: A single centre experience. Asian Biomed., 6: 27-33.
CrossRef  |  

Lin, I.L., M.C. Shih, M.H. Hsieh, T.C. Liu and S.E. Chang et al., 2003. Molecular basis of weak D in Taiwanese. Annl. Hematol., 82: 617-620.
CrossRef  |  Direct Link  |  

Luettringhaus, T.A., D. Cho, D.W. Ryang and W.A. Flegel, 2006. An easy RHD genotyping strategy for D-East Asian persons applied to Korean blood donors. Transfusion, 46: 2128-2137.
CrossRef  |  PubMed  |  Direct Link  |  

Sandler, S.G., W.A. Flegel, C.M. Westhoff, G.A. Denomme and M. Delaney et al., 2015. It's time to phase in RHD genotyping for patients with a serologic weak D phenotype. Transfusion, 55: 680-689.
CrossRef  |  PubMed  |  Direct Link  |  

Shao, C.P., J.H. Maas, Y.Q. Su, M. Kohler and T.J. Legler, 2002. Molecular background of Rh D‐positive, D‐negative, Del and weak D phenotypes in Chinese. Vox Sanguinis, 83: 156-161.
CrossRef  |  Direct Link  |  

Virk, M. and S.G. Sandler, 2015. Rh Immunoprophylaxis for women with a serologic weak D phenotype. Lab. Med., 46: 190-194.
Direct Link  |  

Wafi, M.E., H.E. Housse, N. Nourichafi, K. Bouisk and M. Benajiba et al., 2016. Prevalence of weak D phenotype among D negative C/E+ blood donors in Morocco. Int. J. Blood Transfusion Immunohematology, 6: 3-7.
Direct Link  |  

Wagner, F.F., C. Gassner, T.H. Muller, D. Schonitzer and F. Schunter et al., 1999. Molecular basis of weak D phenotypes. Blood, 93: 385-393.
Direct Link  |  

Yan, L., J. Wu, F. Zhu, X. Hong and X. Xu, 2007. Molecular basis of D variants in Chinese persons. Transfusion, 47: 471-477.
CrossRef  |  PubMed  |  Direct Link  |  

Zacarias, J.M.V., D.F.E.M. Pereira, J.E.L. Visentainer, G.A.S. Guelsin and D.F.C. Melo et al., 2016. Frequency of RHD variants in Brazilian blood donors from Parana State, Southern Brazil. Transfusion Apheresis Sci., 55: 120-124.
PubMed  |  Direct Link  |