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Showing items 1-10 of 43 (5 Page(s) Totally)
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| 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
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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 |
| 臺大學術典藏 |
2022-09-19T07:14:35Z |
Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis
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Hung, Chia-Cheng; Lin, Shin-Yu; Lee, Chien-Nan; Cheng, Hui-Yu; Lin, Chiou-Ya; Chang, Chien-Hui; Chiu, Hsin-Hui; CHIH-CHIEH YU; Lin, Shuan-Pei; Cheng, Wen-Fang; Ho, Hong-Nerng; Niu, Dau-Ming; Su, Yi-Ning |
| 臺大學術典藏 |
2021-03-11T08:16:57Z |
MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia
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Yu, Chih-Hsiang;Lin, Tze-Kang;Jou, Shiann-Tarng;Lin, Chien-Yu;Lin, Kai-Hsin;Lu, Meng-Yao;Chen, Shu-Huey;Cheng, Chao-Neng;Wu, Kang-Hsi;Wang, Shih-Chung;Chang, Hsiu-Hao;Li, Meng-Ju;Ni, Yu-Ling;Su, Yi-Ning;Lin, Dong-Tsamn;Chen, Hsuan-Yu;Harrison, Christine J;Hung, Chia-Cheng;Shu-Wha Lin;Yang, Yung-Li; Yu, Chih-Hsiang; Lin, Tze-Kang; Jou, Shiann-Tarng; Lin, Chien-Yu; Lin, Kai-Hsin; Lu, Meng-Yao; Chen, Shu-Huey; Cheng, Chao-Neng; Wu, Kang-Hsi; Wang, Shih-Chung; Chang, Hsiu-Hao; Li, Meng-Ju; Ni, Yu-Ling; Su, Yi-Ning; Lin, Dong-Tsamn; Chen, Hsuan-Yu; Harrison, Christine J; Hung, Chia-Cheng; SHU-WHA LIN; Yang, Yung-Li |
| 臺大學術典藏 |
2020-05-04T08:08:23Z |
Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan
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Lu, Chun-Yi; Tsao, Po-Nien; Ke, Ying-Ying; Lin, Yi-Hsin; Lin, Yin-Hung; Hung, Chia-Cheng; Su, Yi-Ning; Hsu, Wei-Chung; Hsieh, Wu-Shiun; Huang, Li-Min; Wu, Chen-Chi; Hsu, Chuan-Jen; WEI-CHUNG HSU |
| 臺大學術典藏 |
2019-01-05T07:20:19Z |
Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome
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Kuo, Pei-Wen;Tu, Mei-Pin;Fang, Mei-Ya;Chen, Lang-Yao;Niu, Dau-Ming;Li, Ni-Chung;Lin, Shuan-Pei;Su, Yi-Ning;Hung, Chia-Cheng;Lin, Chiou-Ya;HONG-NERNG HO;WEN-MING HSU;YI-CHING TUNG;WU-SHIUN HSIEH;WEN-YU TSAI;CHIEN-NAN LEE;SHIN-YU LIN; SHIN-YU LIN; CHIEN-NAN LEE; Hung, Chia-Cheng; WEN-YU TSAI; Lin, Shuan-Pei; Li, Ni-Chung; WU-SHIUN HSIEH; YI-CHING TUNG; Niu, Dau-Ming; WEN-MING HSU; Chen, Lang-Yao; Fang, Mei-Ya; Tu, Mei-Pin; Kuo, Pei-Wen; Lin, Chiou-Ya; Su, Yi-Ning; HONG-NERNG HO |
| 臺大學術典藏 |
2018-09-10T15:34:29Z |
Motion analysis of axial rotation and gait stability during turning in people with Parkinson's disease
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Su, Yi-Ning;Lin, Kwan-Hwa;Lee, Chien-Nan;Lin, Kwan-Hwa;Lin, Kwan-Hwa;Shin, Jin-Chung;Lu, Tung-Wu;Lu, Tung-Wu;Lu, Tung-Wu;Wu, Ruey-Meei;Wu, Ruey-Meei;Hsu, Wei-Li;Lin, Chia-Hui;Yang, Wen-Chieh;Hung, Chia-Cheng;Wei-Li Hsu;Lin, Kwan-Hwa;Lu, Tung-Wu;Wu, Ruey-Meei;Hsu, Wei-Li;Yang, Wen-Chieh; Yang, Wen-Chieh; Hsu, Wei-Li; Wu, Ruey-Meei; Lu, Tung-Wu; Lin, Kwan-Hwa; WEI-LI HSU; Hung, Chia-Cheng; Yang, Wen-Chieh; Lin, Chia-Hui; Hsu, Wei-Li; Wu, Ruey-Meei; Wu, Ruey-Meei; Lu, Tung-Wu; Lu, Tung-Wu; Lu, Tung-Wu; Shin, Jin-Chung; Lin, Kwan-Hwa; Lin, Kwan-Hwa; Lee, Chien-Nan; Lin, Kwan-Hwa; Su, Yi-Ning |
| 臺大學術典藏 |
2018-09-10T09:27:32Z |
Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)
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Lee, Chien-Nan; Su, Yi-Ning; Shin, Jin-Chung; Lin, Chia-Hui; Lin, Shin-Yu; CHIEN-NAN LEE; SHIN-YU LIN; Hung, Chia-Cheng; 林芯?;蘇怡寧;李建南;林佳慧; Hung, Chia-Cheng;Lin, Chia-Hui;Lin, Shin-Yu;Shin, Jin-Chung;Lee, Chien-Nan;Su, Yi-Ning; Hung, C.-C. and Lin, C.-H. and Lin, S.-Y. and Shin, J.-C. and Lee, C.-N. and Su, Y.-N. |
| 臺大學術典藏 |
2018-09-10T07:23:46Z |
Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis
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Hung, C.-C. and Lin, S.-Y. and Lee, C.-N. and Cheng, H.-Y. and Lin, C.-Y. and Chang, C.-H. and Chiu, H.-H. and Yu, C.-C. and Lin, S.-P. and Cheng, W.-F. and Ho, H.-N. and Niu, D.-M. and Su, Y.-N.; 洪加政;林芯;李建南;鄭惠予;林久雅;張千慧;邱馨慧;游治節;林炫沛;鄭文芳;何弘能;牛道明;蘇怡寧; HUNG, CHIA-CHENG;LIN, SHIN-YU;LEE, CHIEN-NAN;CHENG, HUI-YU;LIN, CHIOU-YA;CHANG, CHIEN-HUI;CHIU, HSIN-HUI;YU, CHIH-CHIEH;LIN, SHUAN-PEI;CHENG, WEN-FANG;HO, HONG-NERNG;NIU, DAU-MING;SU, YI-NING; SHIN-YU LIN; HONG-NERNG HO; WEN-FANG CHENG; CHIH-CHIEH YU; CHIEN-NAN LEE; HUNG, CHIA-CHENG; LIN, SHIN-YU; LEE, CHIEN-NAN; CHENG, HUI-YU; LIN, CHIOU-YA; CHANG, CHIEN-HUI; CHIU, HSIN-HUI; YU, CHIH-CHIEH; LIN, SHUAN-PEI; CHENG, WEN-FANG; HO, HONG-NERNG; NIU, DAU-MING; SU, YI-NING |
| 臺大學術典藏 |
2018-09-10T07:11:38Z |
Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison
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洪加政;李建南;林佳儀;鄭文芳;陳祈安;謝松蒼;楊智超;鐘育志;蘇怡寧;林文澧; Hung, C.-C. and Lee, C.-N. and Lin, C.-Y. and Cheng, W.-F. and Chen, C.-A. and Hsieh, S.-T. and Yang, C.-C. and Jong, Y.-J. and Su, Y.-N. and Lin, W.-L.; HUNG, CHIA-CHENG;LEE, CHIEN-NAN;LIN, CHIA-YUN;CHENG, WEN-FANG;CHEN, CHI-AN;HSIEH, SUNG-TSANG;YANG, CHIH-CHAO;JONG, YUH- JYH;SU, YI-NING;LIN, WIN-LI; CHI-AN CHEN; WEN-FANG CHENG; SUNG-TSANG HSIEH; CHIEN-NAN LEE; Chih-Chao Yang; HUNG, CHIA-CHENG; LEE, CHIEN-NAN; LIN, CHIA-YUN; CHENG, WEN-FANG; CHEN, CHI-AN; HSIEH, SUNG-TSANG; YANG, CHIH-CHAO; JONG, YUH- JYH; SU, YI-NING; LIN, WIN-LI |
| 臺大學術典藏 |
2018-09-10T05:46:23Z |
Molecular and clinical analyses of 84 patients with tuberous sclerosis complex
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Horng-Huei Liou; Pau-Chung CHEN; Su, Yi-Ning; Chien, Shu-Chin; WANG-TSO LEE; CHIEN-NAN LEE; Liou, Horng-Huei; Chen, Chih-Chuan; Chen, Pau-Chung; Hsieh, Chia-Jung; Chen, Chih-Ping; Lee, Wang-Tso; Lin, Win-Li; Lee, Chien-Nan; Hung, C.-C. and Su, Y.N. and Chien, S.-C. and Liou, H.-H. and Chen, C.-C. and Chen, P.-C. and Hsieh, C.-J. and Chen, C.-P. and Lee, W.-T. and Lin, W.-L. and Lee, C.-N.; Hung, Chia-Cheng; Su, Yi-Ning; Chien, Shu-Chin; Liou, Horng-Huei; Chen, Chih-Chuan; Chen, Pau-Chung; Hsieh, Chia-Jung; Chen, Chih-Ping; Lee, Wang-Tso; Lin, Win-Li; Lee, Chien-Nan; Hung, Chia-Cheng |
Showing items 1-10 of 43 (5 Page(s) Totally)
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