These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


385 related items for PubMed ID: 11833677

  • 1. Molecular biology of partial D and weak D: implications for blood bank practice.
    Flegel WA, Wagner FF.
    Clin Lab; 2002; 48(1-2):53-9. PubMed ID: 11833677
    [Abstract] [Full Text] [Related]

  • 2. Molecular genetics of RH.
    Flegel WA, Wagner FF.
    Vox Sang; 2000; 78 Suppl 2():109-15. PubMed ID: 10938938
    [Abstract] [Full Text] [Related]

  • 3. Molecular genetics of RH and its clinical application.
    Flegel WA.
    Transfus Clin Biol; 2006; 13(1-2):4-12. PubMed ID: 16563832
    [Abstract] [Full Text] [Related]

  • 4. Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention.
    Denomme GA, Wagner FF, Fernandes BJ, Li W, Flegel WA.
    Transfusion; 2005 Oct; 45(10):1554-60. PubMed ID: 16181204
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Identification of RHD alleles with the potential of anti-D immunization among seemingly D- blood donors in Upper Austria.
    Polin H, Danzer M, Gaszner W, Broda D, St-Louis M, Pröll J, Hofer K, Gabriel C.
    Transfusion; 2009 Apr; 49(4):676-81. PubMed ID: 19170995
    [Abstract] [Full Text] [Related]

  • 7. Weak D type 1.1 exemplifies another complexity in weak D genotyping.
    Doescher A, Flegel WA, Petershofen EK, Bauerfeind U, Wagner FF.
    Transfusion; 2005 Oct; 45(10):1568-73. PubMed ID: 16181206
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. RHD 1227A is an important genetic marker for RhD(el) individuals.
    Chen JC, Lin TM, Chen YL, Wang YH, Jin YT, Yue CT.
    Am J Clin Pathol; 2004 Aug; 122(2):193-8. PubMed ID: 15323135
    [Abstract] [Full Text] [Related]

  • 15. Molecular basis of weak D in Taiwanese.
    Lin IL, Shih MC, Hsieh MH, Liu TC, Chang SE, Lin CL, Chang JG.
    Ann Hematol; 2003 Oct; 82(10):617-20. PubMed ID: 12898187
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [The family investigation of a weak D type 15 donor].
    Xiong W, Qin JJ, Liu Y, Zhou YY, Shao CP.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb; 24(1):35-7. PubMed ID: 17285541
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany.
    Döscher A, Vogt C, Bittner R, Gerdes I, Petershofen EK, Wagner FF.
    Transfusion; 2009 Sep; 49(9):1803-11. PubMed ID: 19453979
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 20.