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Journal Abstract Search

136 related items for PubMed ID: 1511989

  • 21. The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis.
    Gladson CL, Scharrer I, Hach V, Beck KH, Griffin JH.
    Thromb Haemost; 1988 Feb 25; 59(1):18-22. PubMed ID: 2966450
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  • 30. [A case of recurrent cerebral vein thrombosis with protein C gene mutation identified].
    Sugahara Y, Ono N, Morishita E, Takashima H.
    Rinsho Shinkeigaku; 2018 Dec 21; 58(12):764-766. PubMed ID: 30487363
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  • 31. Three novel PROC gene lesions causing protein C deficiency.
    Hallam PJ, Mannucci P, Tripodi A, Bevan D, Laursen B, Tengborn L, Wacey A, Cooper DN.
    Clin Genet; 1998 Sep 21; 54(3):231-3. PubMed ID: 9788727
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  • 32. Hereditary protein C deficiency with recurrent thrombosis: identification of a missense mutation (C6218T).
    Song KS, Park YS, Choi CR, Kim HK, Park Q, Kim HS.
    J Korean Med Sci; 1998 Apr 21; 13(2):186-90. PubMed ID: 9610620
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  • 33. Combined occurrence of a heterozygous missense mutation in the protein C gene and allelic exclusion of one protein S allele leading to severe venous thrombosis.
    Knoll B, Hach-Wunderle V, Rieger S, Häring D, Mannhalter C.
    Thromb Res; 2001 Jul 01; 103(1):3-8. PubMed ID: 11434940
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  • 36. Heterozygous protein C deficiency associated with multiple congenital hemangiomas--a case report.
    Simioni P, Zanon G, Lazzaro AR, Patrassi GM, Girolami A.
    Angiology; 1991 Apr 01; 42(4):337-42. PubMed ID: 2014924
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  • 40. De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: demonstration of exon skipping by ectopic transcript analysis.
    Berg LP, Grundy CB, Thomas F, Millar DS, Green PJ, Slomski R, Reiss J, Kakkar VV, Cooper DN.
    Genomics; 1992 Aug 01; 13(4):1359-61. PubMed ID: 1505975
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