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Journal Abstract Search

133 related items for PubMed ID: 9657769

  • 1. Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background.
    Huang CH, Chen Y, Reid ME, Seidl C.
    Blood; 1998 Jul 15; 92(2):664-71. PubMed ID: 9657769
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  • 2. The human Rh50 glycoprotein gene. Structural organization and associated splicing defect resulting in Rh(null) disease.
    Huang CH.
    J Biol Chem; 1998 Jan 23; 273(4):2207-13. PubMed ID: 9442063
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  • 3. Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment.
    Huang CH, Liu Z, Cheng G, Chen Y.
    Blood; 1998 Sep 01; 92(5):1776-84. PubMed ID: 9716608
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  • 5. Molecular defects of the RHCE gene in Rh-deficient individuals of the amorph type.
    Chérif-Zahar B, Matassi G, Raynal V, Gane P, Mempel W, Perez C, Cartron JP.
    Blood; 1998 Jul 15; 92(2):639-46. PubMed ID: 9657766
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  • 6. Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency.
    Cherif-Zahar B, Raynal V, Gane P, Mattei MG, Bailly P, Gibbs B, Colin Y, Cartron JP.
    Nat Genet; 1996 Feb 15; 12(2):168-73. PubMed ID: 8563755
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  • 7. Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.
    Silvy M, Beley S, Peyrard T, Ouchari M, Abdelkefi S, Jemni Yacoub S, Chiaroni J, Bailly P.
    Transfusion; 2015 Jun 15; 55(6 Pt 2):1407-10. PubMed ID: 25413218
    [Abstract] [Full Text] [Related]

  • 8. A splicing mutation of the RHAG gene associated with the Rhnull phenotype.
    Kawano M, Iwamoto S, Okuda H, Fukuda S, Hasegawa N, Kajii E.
    Ann Hum Genet; 1998 Mar 15; 62(Pt 2):107-13. PubMed ID: 9759472
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  • 9. Rhmod syndrome: a family study of the translation-initiator mutation in the Rh50 glycoprotein gene.
    Huang C, Cheng GJ, Reid ME, Chen Y.
    Am J Hum Genet; 1999 Jan 15; 64(1):108-17. PubMed ID: 9915949
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  • 13. Rh-deficiency of the regulator type caused by splicing mutations in the human RH50 gene.
    Chérif-Zahar B, Matassi G, Raynal V, Gane P, Delaunay J, Arrizabalaga B, Cartron JP.
    Blood; 1998 Oct 01; 92(7):2535-40. PubMed ID: 9746795
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  • 14. RH blood group system and molecular basis of Rh-deficiency.
    Cartron JP.
    Baillieres Best Pract Res Clin Haematol; 1999 Dec 01; 12(4):655-89. PubMed ID: 10895258
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  • 15. First report of Rhnull individuals in the Indian population and characterization of the underlying molecular mechanisms.
    Kulkarni SS, Vasantha K, Gogri H, Parchure D, Madkaikar M, Férec C, Fichou Y.
    Transfusion; 2017 Aug 01; 57(8):1944-1948. PubMed ID: 28470789
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  • 16. A novel frameshift mutation in RHAG leads to Rhnull phenotype in a Chinese individual.
    Qing Y, Zou HM, Liu BJ, Cui DL, Yang JH, Huang X.
    Transfusion; 2024 May 01; 64(5):789-792. PubMed ID: 38562113
    [Abstract] [Full Text] [Related]

  • 17. Advance in the Rh blood group system.
    Kajii E.
    Nihon Hoigaku Zasshi; 1998 Feb 01; 52(1):1-18. PubMed ID: 9591398
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  • 18. Biochemical aspects of the blood group Rh (rhesus) antigens.
    Anstee DJ, Tanner MJ.
    Baillieres Clin Haematol; 1993 Jun 01; 6(2):401-22. PubMed ID: 8043932
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  • 19. [Molecular approaches to the Rh blood group system].
    Kajii E.
    Nihon Hoigaku Zasshi; 2006 Oct 01; 60(2):110-9. PubMed ID: 17134012
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