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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Institution Date Title Author
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
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 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 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 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 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 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) 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 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 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 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
國立交通大學 2017-04-21T06:56:50Z Probable high prevalence of limb-girdle muscular dystrophy type 2D in Taiwan Liang, Wen-Chen; Chou, Po-Ching; Hung, Chia-Cheng; Su, Yi-Ning; Kan, Tsu-Min; Chen, Wan-Zi; Hayashi, Yukiko K.; Nishino, Ichizo; Jong, Yuh-Jyh
國立臺灣大學 2015 胚胎著床前基因診斷與遺傳性疾病帶因者篩檢及新生兒基因檢測之臨床應用 洪加政; Hung, Chia-Cheng
國立臺灣大學 2015 Targeted next-generation sequencing of cancer genes identified frequent TP53 and ATRX mutations in leiomyosarcoma Yang, Ching-Yao; Liau, Jau-Yu; Huang, Wei-Ju; Chang, Yu-Ting; Chang, Ming-Chu; Lee, Jen-Chieh; Tsai, Jia-Huei; Su, Yi-Ning; Hung, Chia-Cheng; Jeng, Yung-Ming; 鄭永銘; 李仁傑; 蔡佳惠; 章明珠; 楊卿堯; 張毓廷; 廖肇裕
國立臺灣大學 2012 Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH) Hung, Chia-Cheng; Lin, Chia-Hui; Lin, Shin-Yu; Shin, Jin-Chung; Lee, Chien-Nan; Su, Yi-Ning; 林芯?; 蘇怡寧; 李建南; 林佳慧
國立成功大學 2011-10 IKZF1 deletions predict a poor prognosis in children with B-cell progenitor acute lymphoblastic leukemia: A multicenter analysis in Taiwan Yang, Yung-Li; Hung, Chia-Cheng; Chen, Jiann-Shiuh; Lin, Kai-Hsin; Jou, Shiann-Tarng; Hsiao, Chih-Cheng; Sheen, Jiunn-Ming; Cheng, Chao-Neng; Wu, Kang-Hsi; Lin, Shu-Rung; Yu, Sung-Liang; Chen, Hsuan-Yu; Lu, Meng-Yao; Wang, Shih-Chung; Chang, Hsiu-Hao; Lin, Shu-Wha; Su, Yi-Ning; Lin, Dong-Tsamn
國立臺灣大學 2009 Mutation Spectrum of the Fibrillin-1 (Fbn1) Gene in Taiwanese Patients with Marfan Syndrome 洪加政; 李建南; 鄭惠予; 林炫沛; 陳銘仁; 陳持平; 張千慧; 游治節; 邱馨慧; 鄭文芳; 何弘能; 牛道明; 蘇怡寧; HUNG, CHIA-CHENG; LEE, CHIEN-NAN; CHENG, HUI-YU; LIN, SHUAN-PEI; CHEN, MING-REN; CHEN, CHIH-PING; CHANG, CHIEN-HUI; YU, CHIH- CHIEH; CHIU, HSIN-HUI; CHENG, WEN-FANG; HO, HONG-NERNG; NIU, DAU-MING; SU, YI-NING
國立臺灣大學 2009 Identification of Fibrillin-1 Gene Mutations in Marfan Syndrome by High- Resolution Melting Analysis 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
國立臺灣大學 2009 Identification of Cpg Methylation of the Snrpn Gene by Methylation- Specific Multiplex Pcr 洪加政; 林芯伃; 林炫沛; 牛道明; 李妮鍾; 鄭文芳; 陳持平; 林文澧; 李建南; 蘇怡寧; HUNG, CHIA-CHENG; LIN, SHIN-YU; LIN ,SHUAN-PEI; NIU, DAU-MING; LEE, NI-CHUNG; CHENG, WEN-FANG; CHEN, CHIH-PING; LIN, WIN-LI; LEE, CHIEN-NAN; SU, YI-NING
國立臺灣大學 2009 Interaction between Phox2b and Crebbp Mediates Synergistic Activation: Mechanistic Implications of Phox2b Mutants 蘇怡寧; 洪加政; 謝武勳; 吳國瑞; SU, YI-NING; HUNG, CHIA-CHENG; HSIEH, WU-SHIUN; WU, KOU-JUEY
國立臺灣大學 2008 Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis Hung, Chia-Cheng; Lee, Chien-Nan; Chang, Chien-Hui; Jong, Yuh-Jyh; Chen, Chih-Ping; Hsieh, Wu-Shiun; Su, Yi-Ning; Lin, Win-Li; 洪加政; 李建南; 張千慧; 鐘育志; 陳持平; 謝武勳; 蘇怡寧; 林文澧
國立臺灣大學 2008 Identification of Deletion and Duplication Genotypes of the Pmp22 Gene Using Pcr-Rflp, Competitive Multiplex Pcr, and Multiplex Ligation- Dependent Probe Amplification: A Comparison 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, 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
國立臺灣大學 2008 Comparison of the Mismatch-Specific Endonuclease Method and Denaturing High-Performance Liquid Chromatography for the Identification of Hbb Gene Mutations 洪加政; 蘇怡寧; 林嘉芸; 張吟妃; 張千慧; 鄭文芳; 陳祈安; 李建南; 林文澧; HUNG, CHIA-CHENG; SU, YI-NING; LIN, CHIA-YUN; CHANG, YIN-FEI; CHANG, CHIEN-HUI; CHENG, WEN-FANG; CHEN, CHI-AN; LEE, CHIEN-NAN; LIN, WIN-LI
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
國立臺灣大學 2008 Rapid Prenatal Diagnosis of Spinal Muscular Atrophy by Denaturing High- Performance Liquid Chromatography System 蕭勝文; 鄭博仁; 張舜智; 林玉婷; 洪加政; 陳持平; 蘇怡寧; SHAW, SHENG-WEN; CHENG, PO-JEN; CHANG, SHUENN-DYH; LIN, YU-TING; HUNG, CHIA-CHENG; CHEN, CHIH-PING; SU, YI-NING
國立成功大學 2007-03 Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE Hung, Chia-Cheng; Su, Yi-Ning; Tsao, Po-Nien; Chen, Pau-Chung; Lin, Shio-Jean; Lin, Cheng-Hui; Mu, Shu-Chi; Liu, Chieh-An; Chang, Ying-Chao; Lin, Win-Li; Hsieh, Wu-Shiun; Hsu, Su-Ming

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