| 亞洲大學 |
2002 |
Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan
|
Shi YR;Wu,Jer-Yuarn;Hsu YA;Cheng-Chun Lee;Chang-Hai Tsai;Fuu-Jen Tsai |
| 中國醫藥大學 |
2002 |
Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan
|
Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ |
| 中國醫藥大學 |
2002 |
Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan
|
Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ |
| 中國醫藥大學 |
2002 |
Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan
|
施怡如(Shi YR); 鄔哲源; (Hsu YA); 李正淳(Cheng-Chun Lee); 蔡長海(Chang-Hai Tsai); 蔡輔仁(Fuu-Jen Tsai)* |
| 臺大學術典藏 |
2020-04-24T01:34:23Z |
Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome
|
Wang S.-H.; Chen-Chi Wu; Lu Y.-C.; Lin Y.-H.; Su Y.-N.; Hwu W.-L.; Yu I.-S.; Hsu C.-J. |
| 臺大學術典藏 |
2020-12-16T02:25:37Z |
Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome
|
Wang S.-H.; Wu C.-C.; Lu Y.-C.; Lin Y.-H.; Su Y.-N.; WUH-LIANG HWU; Yu I.-S.; Hsu C.-J. |
| 國家衛生研究院 |
2016-03 |
Mutation spectra of common cancer-associated genes in different phenotypes of colorectal carcinoma without distant metastasis
|
Chang, SC;Lin, PC;Lin, JK;Lin, CH;Yang, SH;Liang, WY;Chen, WS;Jiang, JK |
| 國立臺灣大學 |
2004 |
Mutation Spectrum in Taiwanese Patients with Phenylalanine Hydroxylase Deficiency and a Founder Effect for the R241c Mutation
|
簡穎秀; 蔣書娟; 黃愛珠; 周西平; 曾思珊; 黃淵德; 胡務亮; CHIEN, YIN-HSIU; CHIANG, SHU-CHUAN; HUANG, AI-CHU; CHOU, SHI-PING; TSENG, SZU-SAN; HUANG, YUAN-TE; HWU, WUH-LIANG |
| 臺大學術典藏 |
2020-12-16T02:26:14Z |
Mutation spectrum in Taiwanese patients with phenylalanine hydroxylase deficiency and a founder effect for the R241C mutation.
|
Chien Y.H.;Chiang S.C.;Huang A.;Chou S.P.;Tseng S.S.;Huang Y.T.;Wuh-Liang Hwu; Chien Y.H.; Chiang S.C.; Huang A.; Chou S.P.; Tseng S.S.; Huang Y.T.; WUH-LIANG HWU |
| 臺大學術典藏 |
2020-12-24T06:17:19Z |
Mutation spectrum in Taiwanese patients with phenylalanine hydroxylase deficiency and a founder effect for the R241C mutation.
|
YIN-HSIU CHIEN; Chiang S.C.; Huang A.; Chou S.P.; Tseng S.S.; Huang Y.T.; Hwu W.L. |
| 國立臺灣大學 |
2008-06 |
Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM
|
Lin, SY; Su, YN; Hung, CC; Tsay, W; Chiou, SS; Chang, CT; Ho, HN; Lee, CN |
| 國立臺灣大學 |
2008 |
Mutation Spectrum of 122 Hemophilia a Families from Taiwanese Population by Ld-Pcr, Dhplc, Multiplex Pcr and Evaluating the Clinical Application of Hrm
|
林芯伃; 蘇怡寧; 洪加政; 蔡偉; 邱世欣; 張傑婷; 何弘能; 李建南; LIN, SHIN-YU; SU, YI-NING; HUNG, CHIA-CHENG; TSAY, WOEI; CHIOU, SHYH-SHIN; CHANG, CHIEH-TING; HO, HONG-NERNG; LEE, CHIEN-NAN |
| 臺大學術典藏 |
2018-09-10T07:14:00Z |
Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM
|
Lin, S.-Y. and Su, Y.-N. and Hung, C.-C. and Tsay, W. and Chiou, S.-S. and Chang, C.-T. and Ho, H.-N. and Lee, C.-N.; SHIN-YU LIN; HONG-NERNG HO; CHIEN-NAN LEE |
| 臺大學術典藏 |
2020-02-12T04:06:07Z |
Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM
|
CHIEN-NAN LEE;Ho H.-N;Chang C.-T;Chiou S.-S;Tsay W;Hung C.-C;Su Y.-N;Lin S.-Y; Lin S.-Y; Su Y.-N; Hung C.-C; Tsay W; Chiou S.-S; Chang C.-T; Ho H.-N; CHIEN-NAN LEE |
| 臺大學術典藏 |
2020-02-17T07:43:43Z |
Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM
|
Lin S.-Y;Su Y.-N;Hung C.-C;Tsay W;Chiou S.-S;Chang C.-T;Hong-Nerng Ho;Lee C.-N.; Lin S.-Y; Su Y.-N; Hung C.-C; Tsay W; Chiou S.-S; Chang C.-T; HONG-NERNG HO; Lee C.-N. |
| 臺大學術典藏 |
2021-02-04T06:04:59Z |
Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM
|
Lin S.-Y.;Su Y.-N.;Hung C.-C.;Tsay W.;Chiou S.-S.;Chang C.-T.;Ho H.-N.;Chien-Nan Lee; Lin S.-Y.; Su Y.-N.; Hung C.-C.; Tsay W.; Chiou S.-S.; Chang C.-T.; Ho H.-N.; CHIEN-NAN LEE |
| 臺北醫學大學 |
2005 |
Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateal absence of the vas deferns
|
吳建志; Wu CC |
| 臺北醫學大學 |
2005 |
Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens
|
吳建志; Wu CC; Alper OM; Lu JF; Wang SP; Guo L; Chiang HS; Wong LJ |
| 臺北醫學大學 |
2005 |
Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens
|
吳建志; Wu CC; Alper OM; Wang SP; Guo L; Chiang HS; Wong LJ |
| 國立臺灣大學 |
2003 |
Mutation Spectrum of the Connexin 26 (Gjb2) Gene in Taiwanese Patients with Prelingual Deafness
|
華筱玲; 柯滄銘; 許權振; HWA, HSIAO-LIN; KO, TSANG-MING; HSU, CHUAN-JEN |
| 臺大學術典藏 |
2018-09-10T04:24:41Z |
Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deagness
|
Hwa, H.-L. and Ko, T.-M. and Hsu, C.-J. and Huang, C.-H. and Chiang, Y.-L. and Oong, J.-L. and Chen, C.-C. and Hsu, C.-K.; HSIAO-LIN HWA |
| 臺大學術典藏 |
2020-02-03T08:15:24Z |
Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deagness
|
Hsiao-Lin Hwa;Ko T.-M.;Hsu C.-J.;Huang C.-H.;Chiang Y.-L.;Oong J.-L.;Chen C.-C.;Hsu C.-K.; HSIAO-LIN HWA; Ko T.-M.; Hsu C.-J.; Huang C.-H.; Chiang Y.-L.; Oong J.-L.; Chen C.-C.; Hsu C.-K. |
| 臺大學術典藏 |
2018-09-10T07:23:46Z |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Hung, C.-C. and Lin, S.-Y. and Lee, C.-N. and Cheng, H.-Y. and Lin, S.-P. and Chen, M.-R. and Chen, C.-P. and Chang, C.-H. and Lin, C.-Y. and Yu, C.-C. and Chiu, H.-H. and Cheng, W.-F. and Ho, H.-N. and Niu, D.-M. and Su, Y.; SHIN-YU LIN; HONG-NERNG HO; WEN-FANG CHENG; CHIH-CHIEH YU; CHIEN-NAN LEE |
| 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 |
2022-09-19T07:17:43Z |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Hung, Chia-Cheng; Lin, Shin-Yu; Lee, Chien-Nan; Cheng, Hui-Yu; Lin, Shuan-Pei; Chen, Ming-Ren; Chen, Chih-Ping; Chang, Chien-Hui; Lin, Chiou-Ya; CHIH-CHIEH YU; Chiu, Hsin-Hui; Cheng, Wen-Fang; Ho, Hong-Nerng; Niu, Dau-Ming; Su, Yi-Ning |
