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Journal Abstract Search

190 related items for PubMed ID: 12393640

  • 1. Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.
    Noizat-Pirenne F, Lee K, Pennec PY, Simon P, Kazup P, Bachir D, Rouzaud AM, Roussel M, Juszczak G, Ménanteau C, Rouger P, Kotb R, Cartron JP, Ansart-Pirenne H.
    Blood; 2002 Dec 01; 100(12):4223-31. PubMed ID: 12393640
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  • 2. 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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  • 3. 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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  • 4. Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE ceAR allele (ceAR) encodes a partial c antigen.
    Peyrard T, Pham BN, Poupel S, Martin-Blanc S, Auxerre C, Kappler-Gratias S, Bonin P, Rouger P, Le Pennec PY.
    Transfusion; 2009 Nov 01; 49(11):2406-11. PubMed ID: 19624489
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  • 5. Clinically relevant RHD-CE genotypes in patients with sickle cell disease and in African Brazilian donors.
    Gaspardi AC, Sippert EA, De Macedo MD, Pellegrino J, Costa FF, Castilho L.
    Blood Transfus; 2016 Sep 01; 14(5):449-54. PubMed ID: 27177398
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  • 6. RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.
    Westhoff CM, Vege S, Horn T, Hue-Roye K, Halter Hipsky C, Lomas-Francis C, Reid ME.
    Transfusion; 2013 Nov 01; 53(11 Suppl 2):2983-9. PubMed ID: 23772606
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  • 9. Molecular background of D(C)(e) haplotypes within the white population.
    Noizat-Pirenne F, Le Pennec PY, Mouro I, Rouzaud AM, Juszczak G, Roussel M, Lauroua P, Krause C, Rouger P, Cartron JP, Ansart-Pirenne H.
    Transfusion; 2002 May 01; 42(5):627-33. PubMed ID: 12084172
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  • 12. Weakened expression of 'e' owing to concomitant occurrence of Cys16 and Val245 (VS antigen).
    Rodrigues A, Rios M, Costa FF, Saad ST, Pellegrino J, Castilho L.
    Vox Sang; 2004 Feb 01; 86(2):136-40. PubMed ID: 15023184
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  • 13. 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 01; 55(6 Pt 2):1423-31. PubMed ID: 25857637
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  • 18. Molecular characterization of GYPB and RH in donors in the American Rare Donor Program.
    Vege S, Westhoff CM.
    Immunohematology; 2006 Jun 01; 22(3):143-7. PubMed ID: 17105364
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  • 19. Heterogeneous molecular background of the weak C, VS+, hr B-, Hr B- phenotype in black persons.
    Pham BN, Peyrard T, Juszczak G, Dubeaux I, Gien D, Blancher A, Cartron JP, Rouger P, Le Pennec PY.
    Transfusion; 2009 Mar 01; 49(3):495-504. PubMed ID: 19040491
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  • 20. RHD/CE typing by polymerase chain reaction using sequence-specific primers.
    Gassner C, Schmarda A, Kilga-Nogler S, Jenny-Feldkircher B, Rainer E, Müller TH, Wagner FF, Flegel WA, Schönitzer D.
    Transfusion; 1997 Oct 01; 37(10):1020-6. PubMed ID: 9354819
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