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Journal Abstract Search

254 related items for PubMed ID: 29926983

  • 1. Molecular study of Cw /Cx antigens and frequency of Rh phenotypes in southeast Brazilian blood donors.
    Costa SS, Souza Silva TC, Chiba AK, Cruz BR, Langhi Junior DM, Bordin JO.
    J Clin Lab Anal; 2018 Oct; 32(8):e22570. PubMed ID: 29926983
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  • 4. 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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  • 5. RH diversity in Mali: characterization of a new haplotype RHD*DIVa/RHCE*ceTI(D2).
    Ba A, Beley S, Chiaroni J, Bailly P, Silvy M.
    Transfusion; 2015 Jun; 55(6 Pt 2):1423-31. PubMed ID: 25857637
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  • 6. Molecular basis of the RhCW (Rh8) and RhCX (Rh9) blood group specificities.
    Mouro I, Colin Y, Sistonen P, Le Pennec PY, Cartron JP, Le Van Kim C.
    Blood; 1995 Aug 01; 86(3):1196-201. PubMed ID: 7620172
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  • 8. Variant genotypes associated with reduced expression of RhCE antigens among Brazilian blood donors.
    Dezan MR, Oliveira VB, Conrado MCAV, da Rocha MC, Luz F, Gallucci A, Pereira AC, Krieger JE, Rocha V, Mendrone-Junior A, Dinardo CL.
    Transfusion; 2021 Jun 01; 61(6):1923-1931. PubMed ID: 33687082
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  • 9. A Tutsi family harbouring two new RHCE variant alleles and a new haplotype in the Rh blood group system.
    Deleers M, Thonier V, Claes V, Daelemans C, Peyrard T, El Kenz H.
    Vox Sang; 2020 Jul 01; 115(5):451-455. PubMed ID: 32196693
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  • 10. Systematic RH genotyping and variant identification in French donors of African origin.
    Kappler-Gratias S, Auxerre C, Dubeaux I, Beolet M, Ripaux M, Le Pennec PY, Pham BN.
    Blood Transfus; 2014 Jan 01; 12 Suppl 1(Suppl 1):s264-72. PubMed ID: 23867180
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  • 12. RHCE*ceAG (254C>G, Ala85Gly) is prevalent in blacks, encodes a partial ce-phenotype, and is associated with discordant RHD zygosity.
    Westhoff CM, Vege S, Hipsky CH, Horn T, Hue-Roye K, Keller J, Velliquette R, Lomas-Francis C, Chou ST, Reid ME.
    Transfusion; 2015 Nov 01; 55(11):2624-32. PubMed ID: 26173592
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  • 13. Comprehensive phenotypic and molecular investigation of RhD and RhCE variants in Moroccan blood donors.
    El Housse H, El Wafi M, Ouabdelmoumene Z, Zarati F, Alid R, Nourichafi N, Bouisk K, Benajiba M, Férec C, Fichou Y, Habti N.
    Blood Transfus; 2019 Mar 01; 17(2):151-156. PubMed ID: 30418133
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  • 15. A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.
    Lopez GH, McGowan EC, McGrath KA, Abaca-Cleopas ME, Schoeman EM, Millard GM, O'Brien H, Liew YW, Flower RL, Hyland CA.
    Transfusion; 2016 Sep 01; 56(9):2322-30. PubMed ID: 27390888
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  • 16. Molecular basis of the rare gene complex, DIVa(C)-, which encodes four low-prevalence antigens in the Rh blood group system.
    Hipsky CH, Hue-Roye K, Lomas-Francis C, Huang CH, Reid ME.
    Vox Sang; 2012 Feb 01; 102(2):167-70. PubMed ID: 21729099
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  • 17. Prevalence of RHD*DOL and RHCE*ce(818T) in two populations.
    Halter Hipsky C, da Costa DC, Omoto R, Zanette A, Castilho L, Reid ME.
    Immunohematology; 2011 Feb 01; 27(2):66-7. PubMed ID: 22356522
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  • 18. Molecular background of RH in Bastiaan, the RH:-31,-34 index case, and two novel RHD alleles.
    Reid ME, Hipsky CH, Velliquette RW, Lomas-Francis C, Larimore K, Olsen C.
    Immunohematology; 2012 Feb 01; 28(3):97-103. PubMed ID: 23286557
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  • 19. Identification of RHCE and KEL alleles in large cohorts of Afro-Caribbean and Comorian donors by multiplex SNaPshot and fragment assays: a transfusion support for sickle cell disease patients.
    Silvy M, Di Cristofaro J, Beley S, Papa K, Rits M, Richard P, Chiaroni J, Bailly P.
    Br J Haematol; 2011 Jul 01; 154(2):260-70. PubMed ID: 21623766
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  • 20. 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 01; 58(2):317-322. PubMed ID: 29193119
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