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Journal Abstract Search

254 related items for PubMed ID: 20723165

  • 1. Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.
    Silvy M, Simon S, Gouvitsos J, Di Cristofaro J, Ferrera V, Chiaroni J, Bailly P.
    Transfusion; 2011 Feb; 51(2):401-11. PubMed ID: 20723165
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  • 5. Molecular basis of the RHD gene in blood donors with DEL phenotypes in Shanghai.
    Li Q, Hou L, Guo ZH, Ye LY, Yue DQ, Zhu ZY.
    Vox Sang; 2009 Aug; 97(2):139-46. PubMed ID: 19490579
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  • 7. Molecular biology of partial D and weak D: implications for blood bank practice.
    Flegel WA, Wagner FF.
    Clin Lab; 2002 Aug; 48(1-2):53-9. PubMed ID: 11833677
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  • 9. RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany.
    Döscher A, Vogt C, Bittner R, Gerdes I, Petershofen EK, Wagner FF.
    Transfusion; 2009 Sep; 49(9):1803-11. PubMed ID: 19453979
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  • 10. An easy RHD genotyping strategy for D- East Asian persons applied to Korean blood donors.
    Luettringhaus TA, Cho D, Ryang DW, Flegel WA.
    Transfusion; 2006 Dec; 46(12):2128-37. PubMed ID: 17176325
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  • 12. RHD positive among C/E+ and D- blood donors in Denmark.
    Christiansen M, Sørensen BS, Grunnet N.
    Transfusion; 2010 Jul; 50(7):1460-4. PubMed ID: 20456676
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  • 13. RHD alleles in Brazilian blood donors with weak D or D-negative phenotypes.
    Cruz BR, Chiba AK, Moritz E, Bordin JO.
    Transfus Med; 2012 Apr; 22(2):84-9. PubMed ID: 22211984
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  • 14. Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention.
    Denomme GA, Wagner FF, Fernandes BJ, Li W, Flegel WA.
    Transfusion; 2005 Oct; 45(10):1554-60. PubMed ID: 16181204
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  • 15. Evaluation of the applicability and effectiveness of a molecular strategy for identifying weak D and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD*Ψ.
    Dezan MR, Guardalini LGO, Pessoa E, Ribeiro IH, Oliveira VB, Luz F, Novac DR, Gallucci A, Bonifácio S, Gomes F, Levi JE, Pereira AC, Krieger JE, Mendrone-Junior A, Rocha V, Dinardo CL.
    Transfusion; 2018 Feb; 58(2):317-322. PubMed ID: 29193119
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  • 16. The determination of the fetal D status from maternal plasma for decision making on Rh prophylaxis is feasible.
    Müller SP, Bartels I, Stein W, Emons G, Gutensohn K, Köhler M, Legler TJ.
    Transfusion; 2008 Nov; 48(11):2292-301. PubMed ID: 18694461
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  • 17. Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare alleles.
    Fichou Y, Le Maréchal C, Jamet D, Bryckaert L, Ka C, Audrézet MP, Le Gac G, Dupont I, Chen JM, Férec C.
    Transfusion; 2013 Aug; 53(8):1821-8. PubMed ID: 23228153
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  • 19. Molecular background of D-negative phenotype in the Tunisian population.
    Moussa H, Tsochandaridis M, Chakroun T, Jridi S, Abdelneji B, Hmida S, Silvy M, Bailly P, Gabert J, Levy-Mozziconacci A, Jemni-Yacoub S.
    Transfus Med; 2012 Jun; 22(3):192-8. PubMed ID: 22420413
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  • 20. Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture.
    Silvy M, Chapel-Fernandes S, Callebaut I, Beley S, Durousseau C, Simon S, Lauroua P, Dubosc-Marchenay N, Babault C, Mouchet C, Ferrera V, Chiaroni J, Bailly P.
    Transfusion; 2012 Sep; 52(9):2020-9. PubMed ID: 22320258
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