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Journal Abstract Search

186 related items for PubMed ID: 27338008

  • 1.
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  • 2. Application of Multiplex Ligation-Dependent Probe Amplification Assay for Genotyping Major Blood Group Systems Including DEL Variants in the D-Negative Korean Population.
    Kim B, Lee ST, Kim S, Choi JR, Kim HO.
    Ann Lab Med; 2018 Jan; 38(1):32-38. PubMed ID: 29071816
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  • 3. RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification.
    Haer-Wigman L, Veldhuisen B, Jonkers R, Lodén M, Madgett TE, Avent ND, de Haas M, van der Schoot CE.
    Transfusion; 2013 Jul; 53(7):1559-74. PubMed ID: 23043317
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  • 4. RHD genotype and zygosity analysis in the Chinese Southern Han D+, D- and D variant donors using the multiplex ligation-dependent probe amplification assay.
    Ji YL, Luo H, Wen JZ, Haer-Wigman L, Veldhuisen B, Wei L, Wang Z, Ligthart P, Lodén-van Straaten M, Fu YS, van der Schoot CE, Luo GP.
    Vox Sang; 2017 Oct; 112(7):660-670. PubMed ID: 28833187
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  • 6. 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; 12 Suppl 1(Suppl 1):s264-72. PubMed ID: 23867180
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  • 7. Serological screening and genetic analysis of RhCE variants in the Chinese Southern Han donors.
    Jia S, Chen J, Wen J, Wang Z, Wei L, Fu Y, Luo G, Ji Y.
    Transfus Med; 2021 Aug; 31(4):271-276. PubMed ID: 33998062
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  • 9. 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; 55(11):2624-32. PubMed ID: 26173592
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  • 12. From the investigation of RHD-CE hybrid genes to the recognition of RHCE variants and RHD zygosity. Expanding the analysis by QMPSF in Brazilian donors and in patients with sickle cell disease.
    de Paula Vendrame TA, Arnoni CP, Latini FRM, Pereira Cortez AJ, Bénech C, Fichou Y, Castilho L.
    Blood Transfus; 2023 May; 21(3):202-208. PubMed ID: 35848626
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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; 55(6 Pt 2):1423-31. PubMed ID: 25857637
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  • 16. A novel RHCE*ce 48C, 733G allele with Nucleotide 941C in Exon 7 encodes an altered red blood cell e antigen.
    Hue-Roye K, Hipsky CH, Velliquette RW, Fuchisawa A, Lomas-Francis C, Hoppe C, Reid ME.
    Transfusion; 2011 Jan; 51(1):32-5. PubMed ID: 20576012
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  • 17. Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia.
    Ouchari M, Srivastava K, Romdhane H, Jemni Yacoub S, Flegel WA.
    Transfusion; 2018 Feb; 58(2):306-312. PubMed ID: 29193104
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  • 19. RHD and RHCE molecular analysis in weak D blood donors and in patients with Rh antibodies against their own corresponding Rh antigen.
    Souza Silva TC, Cruz BR, Costa SS, Chiba AK, Barros MMO, Langhi DM, Bordin JO.
    Blood Transfus; 2020 Jul; 18(4):295-303. PubMed ID: 32697929
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  • 20. 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; 14(5):449-54. PubMed ID: 27177398
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