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"lee chen chi"
Showing items 26-50 of 59 (3 Page(s) Totally)
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| 東吳大學 |
2012 |
民事醫療糾紛舉證責任之研究 — 以民事訴訟法第277條但書之舉證責任轉換為中心
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李澄奇; Lee, Chen-chi |
| 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 |
| 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 |
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 |
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 |
2010-09 |
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 ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization
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陳持平;Chen, Chih-Ping;Guo, Yung-Ting;Lin, Shuan-Pei;Su, Yi-Ning;Chen, Yann-Jang;Hseuh, Rui-Yuan;Lin, Yi-Hui;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 of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q
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陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Lee, Chen-Chi;Chen, Wen-Lin;Pan, Chen-Wen;Wu, Pei-Chen;Wang, Wayseen |
| 亞洲大學 |
2010-06 |
Deletion 2q37.3->qter and duplication 15q24.3->qter characterized by array CGH in a girl with epilepsy and dysmorphic features
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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, Li-Feng;Lee, Meng-Shan;Wang, Wayseen |
| 亞洲大學 |
2010-06 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18
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陳持平;Chen, Chih-Ping;Lin, Chyi-Chyang;Su, Yi-Ning;Tsai, Fuu-Jen;Chen, Yu-Ting;Chern, Schu-Rern;Lee, Chen-Chi;Town, Dai-Dyi;Chen, Li-Feng;Wu, Pei-Chen;Wang, Wayseen |
| 亞洲大學 |
2010-03 |
Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Lee, Chen-Chi;Wang, Wayseen |
| 亞洲大學 |
2010-03 |
Unbalanced and balanced heterologous Robertsonian translocations involving chromosome 21 at amniocentesis
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Wu, Pei-Chen;Tsai, Fuu-Jen;Lee, Chen-Chi;Town, Dai-Dyi;Chen, Wen-Lin;Chen, Li-Feng;Lee, Meng-Shan;Pan, Chen-Wen;Wang, Wayseen |
| 國立臺灣大學 |
2010 |
Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence in Situ Hybridization and Array Comparative Genomic Hybridization
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陳持平; 林炫沛; 蘇怡寧; 陳燕彰; 吳佩臻; 李貞姫; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; SU, YI-NING; CHEN, YANN-JANG; WU, PEI-CHEN; LEE, CHEN-CHI; WANG, WAYSEEN |
| 國立臺灣大學 |
2010 |
Mosaic Trisomy 7 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses
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陳持平; 蘇怡寧; 陳樹人; 林炫沛; 許瓊心; 蔡輔仁; 王道遠; 吳佩臻; 李貞姫; 陳麗鳳; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; LIN, SHUAN-PEI; HSU, CHYONG-HSIN; TSAI, FUU-JEN; WANG, TAO-YEUAN; WU, PEI-CHEN; LEE, CHEN-CHI; CHEN, LI-FENG; WANG, WAYSEEN |
| 國立臺灣大學 |
2010 |
Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses
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陳持平; 蘇怡寧; 陳樹人; 蔡輔仁; 吳佩臻; 李貞姫; 李孟珊; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WU, PEI-CHEN; LEE, CHEN-CHI; LEE, MENG-SHAN; WANG, WAYSEEN |
| 國立臺灣大學 |
2010 |
Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 18 and Associated with a Reciprocal Translocation Involving Chromosomes 17 and 18
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陳持平; 林齊强; 蘇怡寧; 蔡輔仁; 陳樹人; 李貞姫; 吳佩臻; 王偉信; CHEN, CHIH-PING; LIN, CHYI-CHYANG; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; LEE, CHEN-CHI; WU, PEI-CHEN; WANG, WAYSEEN |
| 國立臺灣大學 |
2010 |
Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 22
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陳持平; 林齊强; 蘇怡寧; 蔡輔仁; 陳樹人; 李貞姫; 吳佩臻; 王偉信; CHEN, CHIH-PING; LIN, CHYI-CHYANG; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; LEE, CHEN-CHI; WU, PEI-CHEN; WANG, WAYSEEN |
Showing items 26-50 of 59 (3 Page(s) Totally)
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