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"su yi ning"的相关文件
显示项目 36-60 / 253 (共11页)
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| 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 |
2018-09-10T06:52:37Z |
CYP1A1 Ile462Val and GSTT1 modify the effect of cord blood cotinine on neurodevelopment at 2 years of age
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Hsieh, Chia-Jung; Liao, Hua-Fang; Wu, Kuen-Yuh; Hsieh, Wu-Shiun; Su, Yi-Ning; Jeng, Suh-Fang; Yu, Shih-Ni; Chen, Pau-Chung; Hsieh, Chia-Jung; SUH-FANG JENG; WU-SHIUN HSIEH; Liao, Hua-Fang; Wu, Kuen-Yuh; KUEN-YU WU; Pau-Chung CHEN; Hsieh, Wu-Shiun; Su, Yi-Ning; Jeng, Suh-Fang; Yu, Shih-Ni; Chen, Pau-Chung |
| 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 |
| 臺大學術典藏 |
2018-09-10T05:20:55Z |
Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms
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CHIANG, FU-TIEN; JUANG, JYH-MING; LIU, YEN-BIN; HO, YI-LWUN; CHEN, WEN-JONE; KO, YU-LIN; LEI, MENG-HUAN; CHEN, SHIH-ANN; WU, MEI-HWAN; LO, HUEY-MING; HUANG, SHOEI-K STEPHEN; LIN, JIUNN-LEE; SU, YI- NING; LAI, LING-PING; JYH-MING Jimmy JUANG; WEN-JONE CHEN; MEI-HWAN WU; YI-LWUN HO; LING-PING LAI; 賴凌平;蘇怡寧;江福田;莊志明;劉言彬;何奕倫;陳文鍾;柯毓麟;雷孟桓;陳適安;吳美環;駱惠銘;黃水坤;林俊立; Lai, L.-P. and Su, Y.-N. and Chiang, F.-T. and Juang, J.-M. and Liu, Y.-B. and Ho, Y.-L. and Chen, W.-J. and Yeh, S.-J. and Wang, C.-C. and Ko, Y.-L. and Wu, T.-J. and Ueng, K.-C. and Lei, M.-H. and Tsao, H.-M. and Chen, S.-A. and Lin, T.-K. and Wu, M.-H. and Lo, H.-M. and Huang, S.K.S. and Lin, J.-L.; LAI, LING-PING;SU, YI- NING;CHIANG, FU-TIEN;JUANG, JYH-MING;LIU, YEN-BIN;HO, YI-LWUN;CHEN, WEN-JONE;KO, YU-LIN;LEI, MENG-HUAN;CHEN, SHIH-ANN;WU, MEI-HWAN;LO, HUEY-MING;HUANG, SHOEI-K STEPHEN;LIN, JIUNN-LEE; FU-TIEN CHIANG |
| 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 |
| 國立交通大學 |
2017-04-21T06:56:37Z |
Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan
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Liang, Wen-Chen; Tian, Xia; Yuo, Chung-Yee; Chen, Wan-Zi; Kan, Tsu-Min; Su, Yi-Ning; Nishino, Ichizo; Wong, Lee-Jun C.; Jong, Yuh-Jyh |
| 亞洲大學 |
2016-10 |
Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentirc inversion
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陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Su, Yi-Ning;Su, Yi-Ning;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Che, Shin-Wen;Town, Dai-Dyi;Town, Dai-Dyi;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 國立交通大學 |
2015-11-26T00:57:04Z |
利用螢光奈米鑽石結合專一性抗體進行癌症幹細胞標誌SSEA-1的標定與追蹤
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蘇逸寧; Su, Yi-Ning; 趙瑞益; Chao, Jui-I |
| 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 |
2015 |
The relationship of neuroimaging findings and neuropsychiatric comorbidities in children with tuberous sclerosis complex
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Huang, Cheng-Hsien; Peng, Steven Shinn-Forng; Weng, Wen-Chin; Su, Yi-Ning; Lee, Wang-Tso; 彭信逢; 李旺祚; 蘇怡寧; 翁妏謹 |
| 亞洲大學 |
2014-03 |
Detection of altered methylation status at 11p15 and 7q32 in placental mesenchymal dysplasia
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Li, Ming-Huei;Lin, Ming-Huei;Wa, Tao-Yeuan;Wang, Tao-Yeuan;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Yu-Ting;Chen, Yu-Ting;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2014-03 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Che, Shee-Uan;Chen, Shee-Uan;Cha, Tung-Yao;Chang, Tung-Yao;Wu, Pei-Chen;Wu, Pei-Chen;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Kuo, Yu-Ling;Kuo, Yu-Ling;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2014-03 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15
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陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Chern, Schu-Rern;Wu, Peih-Shan;Ch, Shun-Ping;Kuo, Yu-Ling;Chen, Wen-Lin;Wang, Wayseen |
| 臺北醫學大學 |
2014 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15
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Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Chern, Schu-Rern;Wu, Peih-Shan;Chang, Shun-Ping;Kuo, Yu-Ling;Chen, Wen-Lin;Wang, Wayseen |
| 臺北醫學大學 |
2014 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer
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Chen, Chih-Ping;Su, Yi-Ning;Chen, Shee-Uan;Chang, Tung-Yao;Wu, Pei-Chen;Chern, Schu-Rern;Wu, Peih-Shan;Kuo, Yu-Ling;Wang, Wayseen |
| 臺北醫學大學 |
2014 |
Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia
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Chen, Chih-Ping;Su, Yi-Ning;Lin, Ming-Huei;Wang, Tao-Yeuan;Chern, Schu-Rern;Kuo, Yu-Ling;Chen, Yu-Ting;Wang, Wayseen |
| 臺北醫學大學 |
2014 |
PHOX2B Mutation in a Taiwanese Newborn with Congenital Central Hypoventilation Syndrome
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Wang, Tzu-Chiang;Su, Yi-Ning;Lai, Ming-Chi |
| 國立臺灣大學 |
2014 |
Applying the ICF-CY framework to examine biological and environmental factors in early childhood development
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Hwang, Ai-Wen; Liao, Hua-Fang; Chen, Pau-Chung; Hsieh, Wu-Shiun; Simeonsson, Rune J.; Weng, Li-Jen; Su, Yi-Ning; 陳保中; 謝武勳; 蘇怡寧; 廖華芳 |
| 亞洲大學 |
201310 |
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review
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陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Su, Yi-Ning;Hua, Jian-Pei;Huang, Jian-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Ch, Shun-Ping;Chang, Shun-Ping;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of
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陳持平;Chen, Chih-Ping;Cha, Tung-Yao;Chang, Tung-Yao;Guo, Wan-Yuo;Guo, Wan-Yuo;Su, Yi-Ning;Su, Yi-Ning;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-10 |
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review
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陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Su, Yi-Ning;Hua, Jian-Pei;Huang, Jian-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Ch, Shun-Ping;Chang, Shun-Ping;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20
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陳持平;Chen, Chih-Ping;Shuenn-Dyh, C;Chang, Shuenn-Dyh;Chueh, Ho-Yen;Chueh, Ho-Yen;Su, Yi-Ning;Su, Yi-Ning;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Li-Feng;Chen, Li-Feng;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Su, Jun-Wei;Su, Jun-Wei;Ch, Schu-Rern;Chern, Schu-Rern;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma and intrauterine growth restriction
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陳持平;Chen, Chih-Ping;Hs, Chin-Yuan;Hsu, Chin-Yuan;Su, Yi-Ning;Su, Yi-Ning;Wa, Tao-Yeuan;Wang, Tao-Yeuan;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Su, Yi-Ning;Su, Yi-Ning;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
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