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Journal Abstract Search

68 related items for PubMed ID: 4272815

  • 21. A Chinese homozygote of familial hypercholesterolemia: identification of a novel C263R mutation in the LDL receptor gene.
    Wang D, Wu B, Li Y, Heng W, Zhong H, Mu Y, Wang J.
    J Hum Genet; 2001; 46(3):152-4. PubMed ID: 11310584
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  • 22. Phenotypic expression of the main histocompatibility complex (DL-A) in randomly selected mongrel dogs. II. Serologically detectable (SD) compatibility, MLC reactivity, and skin allograft survival.
    Ozaki A, Bachvaroff R, Cannon FD, Mollen N, Blumenstock DA, Ayvazian JH, Ferrebee JW, Rapaport FT.
    Transplant Proc; 1973 Dec; 5(4):1781-3. PubMed ID: 4272831
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  • 27. "Pseudo homozygous" activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: report of two cases belonging to two unrelated kindreds.
    Simioni P, Scudeller A, Radossi P, Gavasso S, Girolami B, Tormene D, Girolami A.
    Thromb Haemost; 1996 Mar; 75(3):422-6. PubMed ID: 8701401
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  • 28. Equine lymphocyte antigens in a Welsh pony family.
    Swift RV, Mottironi VD.
    Am J Vet Res; 1982 Oct; 43(10):1859-62. PubMed ID: 6216833
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  • 31. [Lymphocyte mixed culture reaction (LMC) between parents and children with the same HL-A phenotype. Hypothesis of a genetic recognition system].
    Dausset J, Le Brun A, Sasportes M.
    C R Acad Hebd Seances Acad Sci D; 1972 Nov 13; 275(20):2279-82. PubMed ID: 4630937
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  • 35. Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene.
    Herrmann FH, Auerswald G, Ruiz-Saez A, Navarrete M, Pollmann H, Lopaciuk S, Batorova A, Wulff K, Greifswald Factor X Deficiency Study Group.
    Haemophilia; 2006 Sep 13; 12(5):479-89. PubMed ID: 16919077
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  • 36. HL-A antigens and malignant disease.
    Lawler SD.
    Br J Cancer Suppl; 1973 Aug 13; 1():243-9. PubMed ID: 4374228
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