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Showing items 171-195 of 420 (17 Page(s) Totally)
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| 國立臺灣大學 |
2011 |
Identification of Novel Susceptibility Loci for Kawasaki Disease in a Han Chinese Population by a Genome-Wide Association Study
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蔡輔仁; 李宜靜; 張正成; 黃立民; 黃富源; 邱南昌; 陳銘仁; 紀鑫; 李燕晉; 劉怡敏; 陳建勳; 陳垣崇; 鄔哲源; TSAI, FUU-JEN; LEE, YI-CHING; CHANG, JENG- SHENG; HUANG, LI-MIN; HUANG, FU-YUAN; CHIU, NAN- CHANG; CHEN, MING-REN; CHI, HSIN; LEE, YEN-CHING; LIU, YI-MIN; CHEN, CHIEN-HSIUN; CHEN, YUAN-TSONG; WU, JER-YUARN |
| 國立臺灣大學 |
2011 |
Mosaic Supernumerary R(1)(P13.2q23.3) in a 10-Year-Old Girl with Epilepsy, Facial Asymmetry, Psychomotor Retardation, Kyphoscoliosis, Dermatofibrosarcoma and Multiple Exostoses
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陳持平; 林炫沛; 陳明; 蘇怡寧; 陳樹人; 王道遠; 劉育朋; 蔡輔仁; 李貞?; 陳燕彰; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; CHEN, MING; SU, YI-NING; CHERN, SCHU-RERN; WANG, TAO-YEUAN; LIU, YU-PENG; TSAI, FUU-JEN; LEE, CHEN-CHI; CHEN, YANN-JANG; WANG, WAYSEEN |
| 國立臺灣大學 |
2011 |
Prenatal Diagnosis and Molecular Cytogenetic Characterization of Mosaicism for a Small Supernumerary Marker Chromosome Derived from Ring Chromosome 4
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陳持平; 陳明; 蘇怡寧; 蔡輔仁; 陳樹人; 吳佩臻; 陳麗鳳; 王偉信; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; CHEN, LI-FENG; WANG, WAYSEEN |
| 國立臺灣大學 |
2011 |
Prenatal Diagnosis of Mosaic Trisomy 8: Clinical Report and Literature Review
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陳持平; 陳明; 潘怡如; 蘇怡寧; 陳樹人; 蔡輔仁; 王偉信; CHEN, CHIH-PING; CHEN, MING; PAN, YI-JU; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN |
| 國立臺灣大學 |
2011 |
Impact of Shock Wave Lithotripsy on Heart Rate Variability in Patients with Urolithiasis
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林武周; 何建宜; 陳永祥; 陳慧毅; 蔡輔仁; 沈瑞隆; 黃柏勳; 陳玉怜; 文寄銘; 陳汶吉; LIN, WU-CHOU; HO, CHIEN-YI; CHEN, YUNG-HSIANG; CHEN, HUEY-YI; TSAI, FUU-JEN; SHEN, JUI-LUNG; HUANG, PO-HSUN; CHEN, YUH-LIEN; MAN, KEE-MING; CHEN, WEN-CHI |
| 國立臺灣大學 |
2011 |
Subunit 6 of the Cop9 Signalosome Promotes Tumorigenesis in Mice through Stabilization of Mdm2 and Is Upregulated in Human Cancers
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陳佑宗; 賴建成; 蔡輔仁; 李孟鴻; CHEN, YOU-TZUNG; LAI, CHIEN-CHEN; TSAI, FUU-JEN; LEE, MONG-HONG |
| 亞洲大學 |
2010-12 |
A 5.3-Mb duplication of 9p12->p13.1 characterized by array CGH in a female infant with developmental delay
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陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Tsai, Fuu-Jen;Lee, Chen-Chi;Pan, Chen-Wen;Wu, Pei-Chen;Wang, Wayseen |
| 亞洲大學 |
2010-12 |
Balanced reciprocal translocations at amniocentesis
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陳持平;Chen, Chih-Ping;Wu, Pei-Chen;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Lee, Chen-Chi;Town, Dai-Dyi;Chen, Wen-Lin;Chen, Li-Feng;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2010-12 |
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
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陳持平;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Hsu, Chin-Yuan;Tsai, Fuu-Jen;Chern, Schu-Rern;Wu, Pei-Chen;Lee, Chen-Chi;Wang, Wayseen |
| 亞洲大學 |
2010-12 |
Key Features for Designing Phosphodiesterase-5 Inhibitors
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;Chang, Tung-Ti;Huang, Hung-Jin;李桂仁;Lee, Kuei-Jen;Yu, Hsin Wei;Chen, Hsin-Yi;蔡輔仁;Tsai, Fuu-Jen;Sun, Mao-Feng;陳語謙;Chen, Calvin Yu-Chian |
| 亞洲大學 |
2010-12 |
Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea
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陳持平;Chen, Chih-Ping;Chiang, Ming-Chou;Wang, Tzu-Hao;Hsueh, Chuen;Chang, Shueen-Dyh;Tsai, Fuu-Jen;Wang, Chao-Ning;Chern, Schu-Rern;Wang, Wayseen |
| 亞洲大學 |
2010-12 |
Partial trisomy 10q (10q25.1->qter) and partial monosomy 13q (13q34->qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Chern, Schu-Rern;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Wen-Lin;Wang, Wayseen |
| 亞洲大學 |
2010-12 |
Partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Young, Richard Shih-Hung;Tsai, Fuu-Jen;Wu, Pei-Chen;Chern, Schu-Rern;Town, Dai-Dyi;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2010-12 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8
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陳持平;Chen, Chih-Ping;Chen, Ming;Ko, Tsang-Ming;Ma, Gwo-Chin;Tsai, Fuu-Jen;Tsai, Ming-Song;Wu, Pei-Chen;Lee, Chen-Chi;Che, Li-Feng;Wang, Wayseen |
| 亞洲大學 |
2010-12 |
Prenatal diagnosis of partial monosomy 1q (1q42.3->qter) associated with hydrocephalus and corpus callosum agenesis
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Lin, Hung-Hung;Wu, Pei-Chen;Lee, Chen-Chi;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2010-12 |
Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling
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陳持平;Chen, Chih-Ping;Huang, Ming-Chao;Su, Yi-Ning;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Town, Dai-Dyi;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2010-11 |
Current Development of Computer-Aided Drug Design
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;Huang, Hung-Jin;Yu, Hsin Wei;Chen, Chien-Yu;Hsu, Chih-Ho;Chen, Hsin-Yi;李桂仁;Lee, Kuei-Jen;蔡輔仁;Tsai, Fuu-Jen;陳語謙;Chen, Calvin Yu-Chian |
| 亞洲大學 |
2010-11 |
Current developments of computer-aided drug design
|
李桂仁;Lee, Kuei-Jen;蔡輔仁;Tsai, Fuu-Jen;陳語謙;Chen, Calvin Yu-Chian |
| 亞洲大學 |
2010-10 |
A Novel Strategy for Designing the Selective PPAR Agonist by the “Sum of Activity” Model
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;Huang, Hung-Jin;李桂仁;Lee, Kuei-Jen;Yu, Hsin Wei;Chen, Hsin-Yi;Tsai, Fuu-Jen;陳語謙;Chen, Calvin Yu-Chian |
| 亞洲大學 |
2010-09 |
A de novo 7.9 Mb deletion in 22q13.2->qter in a boy with autistic features, epilepsy, developmental delay atopic dermatitis and abnormal immunological findings
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陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Wang, Wayseen |
| 亞洲大學 |
2010-09 |
Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chern, Schu-Rern;Hwu, Yu-Ming;Lin, Shuan-Pei;Hsu, Chyong-Hsin;Tsai, Fuu-Jen;Wang, Tao-Yeuan;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Chen, Li-Feng;Wang, Wayseen |
| 亞洲大學 |
2010-09 |
Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses
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陳持平;Chen, Chih-Ping;Lin, Hsien-Ming;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chen, Yu-Ting;Lee, Meng-Shan;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2010-09 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21
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陳持平;Chen, Chih-Ping;Lin, Chyi-Chyang;Ko, Tsang-Ming;Tsai, Fuu-Jen;Chern, Schu-Rern;Lee, Chen-Chi;Chen, Yu-Ting;Wu, Pei-Chen;Wang, Wayseen |
| 亞洲大學 |
2010-09 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22
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陳持平;Chen, Chih-Ping;Lin, Chyi-Chyang;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Lee, Chen-Chi;Chen, Wen-Ling;Chen, Li-Feng;Wu, Pei-Chen;Wang, Wayseen |
| 亞洲大學 |
2010-09 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly
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陳持平;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Tsai, Fuu-Jen;Chern, Schu-Rern;Hsu, Chin-Yuan;Wu, Pei-Chen;Town, Dai-Dyi;Lee, Dong-Jay;Ma, Gwo-Chin;Wang, Wayseen |
Showing items 171-195 of 420 (17 Page(s) Totally)
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