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Showing items 221-230 of 307  (31 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-02-17T07:43:41Z Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome Hung C.-C; Lin S.-Y; Lee C.-N; Cheng H.-Y; Lin S.-P; Chen M.-R; Chen C.-P; Chang C.-H; Lin C.-Y; Yu C.-C; Chiu H.-H; Cheng W.-F; HONG-NERNG HO; Niu D.-M; Su Y.
臺大學術典藏 2020-02-17T07:43:41Z Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis Hung C.-C;Lin S.-Y;Lee C.-N;Cheng H.-Y;Lin C.-Y;Chang C.-H;Chiu H.-H;Yu C.-C;Lin S.-P;Cheng W.-F;Hong-Nerng Ho;Niu D.-M;Su Y.-N.; Hung C.-C; Lin S.-Y; Lee C.-N; Cheng H.-Y; Lin C.-Y; Chang C.-H; Chiu H.-H; Yu C.-C; Lin S.-P; Cheng W.-F; HONG-NERNG HO; Niu D.-M; Su Y.-N.
臺大學術典藏 2020-02-14T02:50:02Z Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin S.-P.; Chen M.-R.; Chen C.-P.; Chang C.-H.; Lin C.-Y.; Yu C.-C.; Chiu H.-H.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.
臺大學術典藏 2020-02-14T02:50:02Z Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin C.-Y.; Chang C.-H.; Chiu H.-H.; Yu C.-C.; Lin S.-P.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.-N.
臺大學術典藏 2020-02-12T04:06:04Z Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis Su Y.-N.;Niu D.-M;Ho H.-N;Cheng W.-F;Lin S.-P;Yu C.-C;Chiu H.-H;Chang C.-H;Lin C.-Y;Cheng H.-Y;CHIEN-NAN LEE;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y; CHIEN-NAN LEE; Cheng H.-Y; Lin C.-Y; Chang C.-H; Chiu H.-H; Yu C.-C; Lin S.-P; Cheng W.-F; Ho H.-N; Niu D.-M; Su Y.-N.
臺大學術典藏 2020-02-12T04:05:47Z Comparison of 3 risk estimation methods for predicting cardiac outcomes in pregnant women with congenital heart disease Wu M.-H.;CHIEN-NAN LEE;Lin M.-T;Chiu S.-N;Chen C.-A;Wang J.-K;Chiu H.-H;Chen S.-Y;Shih J.-C;Lu C.-W; Lu C.-W; Shih J.-C; Chen S.-Y; Chiu H.-H; Wang J.-K; Chen C.-A; Chiu S.-N; Lin M.-T; CHIEN-NAN LEE; Wu M.-H.
臺大學術典藏 2020-02-06T05:22:16Z Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome Chen C.-P.; Chang C.-H.; Lin C.-Y.; Yu C.-C.; Chiu H.-H.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.; Chen M.-R.; Lin S.-P.; Cheng H.-Y.; Su Y.;Niu D.-M.;Ho H.-N.;WEN-FANG CHENG;Chiu H.-H.;Yu C.-C.;Lin C.-Y.;Chang C.-H.;Chen C.-P.;Chen M.-R.;Lin S.-P.;Cheng H.-Y.;Lee C.-N.;Lin S.-Y.;Hung C.-C.; Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin S.-P.; Chen M.-R.; Chen C.-P.; Chang C.-H.; Lin C.-Y.; Yu C.-C.; Chiu H.-H.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.; Hung C.-C.; Lin S.-Y.; Lee C.-N.
臺大學術典藏 2020-02-06T05:22:16Z Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis Su Y.-N.;Niu D.-M.;Ho H.-N.;WEN-FANG CHENG;Lin S.-P.;Yu C.-C.;Chiu H.-H.;Chang C.-H.;Lin C.-Y.;Cheng H.-Y.;Lee C.-N.;Lin S.-Y.;Hung C.-C.; Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin C.-Y.; Chang C.-H.; Chiu H.-H.; Yu C.-C.; Lin S.-P.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.-N.; Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin C.-Y.; Chang C.-H.; Chiu H.-H.; Yu C.-C.; Lin S.-P.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.-N.
臺大學術典藏 2020 Turner syndrome and cardiovascular anomalies: Care for girls and women Chiu H.-H.; YIN-HSIU CHIEN
臺大學術典藏 2020 Exercise Capacity and Ventricular Remodeling after Transcatheter Ventricular Septal Defect Closure in Asymptomatic or Minimally Symptomatic Adolescents and Adults Lin M.-T.; Wang J.-K.; Chen C.-A.; Chen C.-A.;Wang J.-K.;Lin M.-T.;Chiu H.-H.;Hsu J.-Y.;Lin S.-M.;Chang Y.-M.;Chiu S.-N.;Lu C.-W.;Mei-Hwan Wu;Yang M.-C.; Chiu H.-H.; Hsu J.-Y.; Lin S.-M.; Chang Y.-M.; Chiu S.-N.; Lu C.-W.; MEI-HWAN WU; Yang M.-C.

Showing items 221-230 of 307  (31 Page(s) Totally)
<< < 18 19 20 21 22 23 24 25 26 27 > >>
View [10|25|50] records per page