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Journal Abstract Search

354 related items for PubMed ID: 33231305

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    Maheshwari A, Killeen RB.
    ; 2024 01. PubMed ID: 35593798
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  • 28. Lack of Duffy antigen expression is associated with organ damage in patients with sickle cell disease.
    Afenyi-Annan A, Kail M, Combs MR, Orringer EP, Ashley-Koch A, Telen MJ.
    Transfusion; 2008 May; 48(5):917-24. PubMed ID: 18248572
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  • 31. Erythroid urea transporter deficiency due to novel JKnull alleles.
    Wester ES, Johnson ST, Copeland T, Malde R, Lee E, Storry JR, Olsson ML.
    Transfusion; 2008 Feb; 48(2):365-72. PubMed ID: 18028269
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  • 33. Frequencies of genetic variants of the Rh, Kell, Duffy, Kidd, MNS and Diego systems of northwest Rio Grande do Sul, Brazil.
    Soares SDS, Aquino JR, Petrolli F, de Oliveira TB, Almeida S, Fiegenbaum M.
    Hematol Transfus Cell Ther; 2023 Feb; 45(3):317-323. PubMed ID: 35715379
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  • 37. Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K0 (Kellnull ) phenotypes.
    Lomas-Francis C, Vege S, Velliquette RW, Fuchisawa A, Uchikawa M, Tani Y, Moro H, Debnath AK, Westhoff CM.
    Transfusion; 2013 Nov; 53(11 Suppl 2):2887-91. PubMed ID: 23968329
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  • 38. A novel mutation in the coding sequence of the FY*B allele of the Duffy chemokine receptor gene is associated with an altered erythrocyte phenotype.
    Parasol N, Reid M, Rios M, Castilho L, Harari I, Kosower NS.
    Blood; 1998 Oct 01; 92(7):2237-43. PubMed ID: 9746760
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  • 39. Genetic diversity of KELnull and KELel: a nationwide Austrian survey.
    Körmöczi GF, Wagner T, Jungbauer C, Vadon M, Ahrens N, Moll W, Mühlbacher A, Ozgül-Gülce S, Kleinrath T, Kilga-Nogler S, Schönitzer D, Gassner C.
    Transfusion; 2007 Apr 01; 47(4):703-14. PubMed ID: 17381630
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  • 40. Frequency of red blood cell genotypes in multi-transfused patients and blood donors from Minas Gerais, Southeast Brazil.
    Alves VM, De Vito FB, Martins PRJ, Silva SS, Castilho L, Moraes-Souza H.
    Transfus Apher Sci; 2018 Feb 01; 57(1):71-75. PubMed ID: 29330014
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