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Journal Abstract Search

186 related items for PubMed ID: 27338008

  • 21. 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; 115(5):451-455. PubMed ID: 32196693
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  • 22. 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; 61(6):1923-1931. PubMed ID: 33687082
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  • 23. 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; 53(11 Suppl 2):2983-9. PubMed ID: 23772606
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  • 24. Five-Years Review of RHCE Alleles Detected after Weak and/or Discrepant C Results in Southern France.
    Pedini P, Filosa L, Bichel N, Picard C, Silvy M, Chiaroni J, Izard C, Laget L, Mazières S.
    Genes (Basel); 2022 Jun 14; 13(6):. PubMed ID: 35741820
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  • 26. The RHCE allele ceCF: the molecular basis of Crawford (RH43).
    Flegel WA, Wagner FF, Chen Q, Schlanser G, Frame T, Westhoff CM, Moulds MK.
    Transfusion; 2006 Aug 14; 46(8):1334-42. PubMed ID: 16934069
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  • 28. Molecular basis of the Rh antigen RH48 (JAL).
    Hustinx H, Poole J, Bugert P, Gowland P, Still F, Fontana S, Scharberg EA, Tilley L, Daniels G, Niederhauser C.
    Vox Sang; 2009 Apr 14; 96(3):234-9. PubMed ID: 19207167
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  • 29. A novel silent RHCE allele in Chinese population.
    Zhao FY, Li Q, Zhang DM, Guo ZH, Wu YX, Wang F, Zhang JM, Qian M, Zhu ZY.
    Transfus Med; 2019 Dec 14; 29(6):430-433. PubMed ID: 31429112
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  • 32. [Polymorphisms of RHCE gene among serologic RhD negative donors of Han population in Chinese Jiangsu area].
    Chen Q, Xiao JY, Yu X, Huang CY, Yao GH.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2014 Oct 14; 22(5):1428-31. PubMed ID: 25338601
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  • 33. Molecular basis and zygosity determination of D variants including identification of four novel alleles in Chinese individuals.
    He J, Ying Y, Hong X, Xu X, Zhu F, Lv H.
    Transfusion; 2015 Jan 14; 55(1):137-43. PubMed ID: 25070883
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  • 35. RHD*weak partial 4.0 is associated with an altered RHCE*ce(48C, 105T, 733G, 744C, 1025T) allele in the Tunisian population.
    Ouchari M, Polin H, Romdhane H, Abdelkefi S, Houissa B, Chakroun T, Gabriel C, Hmida S, Jemni Yacoub S.
    Transfus Med; 2013 Aug 14; 23(4):245-9. PubMed ID: 23742316
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  • 36. 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 14; 42(5):627-33. PubMed ID: 12084172
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  • 38. The low-prevalence Rh antigen STEM (RH49) is encoded by two different RHCE*ce818T alleles that are often in cis to RHD*DOL.
    Reid ME, Halter Hipsky C, Hue-Roye K, Coghlan G, Olsen C, Lomas-Francis C.
    Transfusion; 2013 Mar 14; 53(3):539-44. PubMed ID: 22738288
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  • 39. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry analysis of 36 blood group alleles among 396 Thai samples reveals region-specific variants.
    Jongruamklang P, Gassner C, Meyer S, Kummasook A, Darlison M, Boonlum C, Chanta S, Frey BM, Olsson ML, Storry JR.
    Transfusion; 2018 Jul 14; 58(7):1752-1762. PubMed ID: 29656499
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  • 40. 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 14; 56(9):2322-30. PubMed ID: 27390888
    [Abstract] [Full Text] [Related]

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