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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Showing items 126-132 of 132 (6 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2021-05-25T06:35:51Z	Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent	MING-CHING SHEN; Chen M.; Chang S.-P.; Lin P.-T.; Hsieh H.-N.; Lin K.-H.
臺大學術典藏	2021-05-25T06:35:51Z	Transfusion-transmitted infection and comorbidities in patients with severe haemophilia: A longitudinal birth cohort analysis	Wang J.-D.;Lin C.-Y.;Weng T.-F.;Chiou S.-S.;Peng C.-T.;Ming-Ching Shen; Wang J.-D.; Lin C.-Y.; Weng T.-F.; Chiou S.-S.; Peng C.-T.; MING-CHING SHEN
臺大學術典藏	2021-05-25T06:35:50Z	Acquired FXIII inhibitor: Patient characteristics and treatment outcome, a case series in Taiwan	Chou S.-C.; Lin C.-Y.; Yen C.-T.; Hsieh H.-N.; Huang Y.-C.; Li K.-J.; Lin S.-W.; MING-CHING SHEN
臺大學術典藏	2021-05-25T06:35:50Z	A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan	Huang Y.-C.;Shih Y.-H.;Lin C.-Y.;Chiu P.-F.;Kuo S.-F.;Lin J.-S.;Ming-Ching Shen; Huang Y.-C.; Shih Y.-H.; Lin C.-Y.; Chiu P.-F.; Kuo S.-F.; Lin J.-S.; MING-CHING SHEN
臺大學術典藏	2021-05-25T06:35:49Z	First reported case of congenital thrombotic thrombocytopenic purpura in Taiwan with novel mutation of ADAMTS13 gene	Chou S.-C.; Lin D.-T.; Lin C.-Y.; Huang Y.-C.; Hsieh H.-N.; MING-CHING SHEN
中原大學	2000	Identification of a new CA dinucleotide repeat in the human factor VIII gene	Shu-Rung Lin;Shu-Wha Lin;Ya-Chu Hsu;Ming-Ching Shen
中原大學	1995	Genetic diagnosis of haemophilia A of Chinese origin	Shu-Rung Lin;Shu-Chuan Chang;Chia-Cheng Lee;Ming-Ching Shen;Shu-Wha Lin

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