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"wu pei chen"
Showing items 101-110 of 127 (13 Page(s) Totally)
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| 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 |
| 國立臺灣大學 |
2010 |
Second-Trimester Molecular Prenatal Diagnosis of Sporadic Apert Syndrome Following Sonographic Findings of Mild Ventriculomegaly and Clenched Hands Mimicking Trisomy 18
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陳持平; 蘇怡寧; 徐金源; 蔡輔仁; 陳樹人; 吳佩臻; 王偉信; 林珮瑩; CHEN, CHIH-PING; SU, YI-NING; HSU, CHIN-YUAN; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; WANG, WAYSEEN; LING, PEI-YING |
| 國立臺灣大學 |
2010 |
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; 陳明; 蘇怡寧; 蔡輔仁; 陳樹人; 徐金源; 吳佩臻; 李東杰; 馬國欽; 王偉信; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; HSU, CHIN-YUAN; WU, PEI-CHEN; LEE, DONG-JAY; MA, GWO-CHIN; WANG, WAYSEEN |
| 國立臺灣大學 |
2010 |
Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings
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陳持平; 陳明; 蘇怡寧; 徐金源; 蔡輔仁; 陳樹人; 吳佩臻; 李貞?; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; HSU, CHIN-YUAN; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; LEE, CHEN-CHI |
| 淡江大學 |
2009-12-15 |
Conversion and degradation of shellfish wastes by Bacillus cereus TKU018 fermentation for the production of chitosanase and bioactive materials
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Wang, San-Lang; Chen, Tz-Rung; Liang, Tzu-Wen; Wu, Pei-Chen |
| 亞洲大學 |
2009-12 |
Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chiang, Shu-Shien;Wang, Wayseen |
Showing items 101-110 of 127 (13 Page(s) Totally)
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