臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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机构	日期	题名	作者
臺大學術典藏	2021-05-25T06:36:09Z	High prevalence of antithrombin III, protein C and protein S deficiency, but no factor V leiden mutation in venous thrombophilic chinese patients in Taiwan	MING-CHING SHEN; Lin J.-S.; Tsay W.
臺大學術典藏	2021-05-25T06:36:08Z	The mutation at position 20210 in the 3'-untranslated region of the prothrombin gene is extremely rare in Taiwanese Chinese patients with venous thrombophilia [2]	Lin J.-S.; MING-CHING SHEN; Tsay W.
臺大學術典藏	2021-05-25T06:36:08Z	Familial macrothrombocytopenia with granulocyte inclusion: A clinical and laboratory problem	Lin J.-S.; MING-CHING SHEN; Wang C.-H.; Lin C.-T.
臺大學術典藏	2021-05-25T06:36:05Z	Protein C and protein S deficiencies are the most important risk factors associated with thrombosis in Chinese venous thrombophilic patients in Taiwan	MING-CHING SHEN; Lin J.-S.; Tsay W.
臺大學術典藏	2021-05-25T06:36:05Z	The prevalence of C677T mutation in the methylenetetrahydrofolate reductase gene and its association with venous thrombophilia in Taiwanese Chinese	Lin J.-S.; MING-CHING SHEN; Tsai W.; Lin B.
臺大學術典藏	2021-05-25T06:36:04Z	Factor V Arg306 → Gly mutation is not associated with activated protein C resistance and is rare in Taiwanese Chinese	MING-CHING SHEN; Lin J.-S.; Tsay W.
臺大學術典藏	2021-05-25T06:36:04Z	Factor V arg306-> Gly is not a risk factor for venous thrombophilia in Taiwanese Chinese	Lin J.S.; MING-CHING SHEN; Tsai W.; Lin B.; Lin B.B.; Hong M.H.
臺大學術典藏	2021-05-25T06:36:03Z	Novel mutations in the factor VII gene of Taiwanese factor VII-deficient patients	MING-CHING SHEN; Lin J.-S.; Lin S.-W.; Yang W.-S.; Lin B.
臺大學術典藏	2021-05-25T06:36:02Z	Age, sex and vitamin status affect plasma level of homocysteine, but hyperhomocysteinaemia is possibly not an important risk factor for venous thrombophilia in Taiwanese Chinese	Lin J.-S.; MING-CHING SHEN; Cheng W.-C.; Tsay W.; Wang Y.-C.; Lin B.-B.; Hung M.-H.
臺大學術典藏	2021-05-25T06:36:01Z	A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation	MING-CHING SHEN; Lin J.-S.; Lin D.S.-Y.; Hsu S.-C.; Lin B.

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