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"hung chia cheng"
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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 |
| 國立交通大學 |
2017-04-21T06:56:50Z |
Probable high prevalence of limb-girdle muscular dystrophy type 2D in Taiwan
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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
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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
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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)
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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
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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
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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
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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
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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
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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
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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
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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, 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
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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
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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
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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
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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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