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"wu pei chen"的相關文件
顯示項目 81-90 / 121 (共13頁)
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| 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 |
Detection and comparison of the levels of cytomegalovirus DNA in amniotic fluid and fetal ascites in a second-trimester fetus with massive ascites, hyperechogenic bowel, ventriculomegaly and intrauterine growth restriction
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Wang, Tao-Yeuan;Tsai, Fuu-Jen;Lin, Hung-Hung;Wu, Pei-Chen;Wang, Wayseen |
| 亞洲大學 |
2010-06 |
Detection of a balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Wu, Chia-Hsun;Tsai, Fuu-Jen;Wu, Pei-Chen;Wang, Wayseen |
| 亞洲大學 |
2010-06 |
Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Huang, Jon-Kway;Liu, Yu-Peng;Tsai, Fuu-Jen;Yang, Chun-Kuang;Huang, Jian-Pei;Chen, Chen-Yu;Wu, Pei-Chen;Wang, Wayseen |
| 亞洲大學 |
2010-06 |
Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Chen, Hsaio-En Cindy;Chiang, Shu-Shien;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 |
Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Hsu, Chin-Yuan;Tsai, Fuu-Jen;Chien, Shu-Chin;Chern, Schu-Rern;Lee, Meng-Shan;Wu, Pei-Chen;Chen, Hsaio-En Cindy;Wang, Wayseen |
| 亞洲大學 |
2010-03 |
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;Chen, Chih-Ping;Su, Yi-Ning;Hsu, Chin-Yuan;Ling, Pei-Ying;Tsai, Fuu-Jen;Chern, Schu-Rern;Wu, Pei-Chen;Chen, Hsaio-En Cindy;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 |
Apert Syndrome Associated with Upper Airway Obstruction and Gastroesophageal Reflux Inducing Polyhydramnios in the Third Trimester
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陳持平; 林炫沛; 蘇怡寧; 陳震宇; 蔡輔仁; 劉育朋; 陳樹人; 吳佩臻; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; SU, YI-NING; CHEN, JEN-YEU; TSAI, FUU-JEN; LIU, YU-PENG; CHERN, SCHU-RERN; WU, PEI-CHEN; WANG, WAYSEEN |
顯示項目 81-90 / 121 (共13頁)
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