|
|
Taiwan Academic Institutional Repository >
Browse by Author
|
"wang wayseen"
Showing items 166-175 of 201 (21 Page(s) Totally)
<< < 12 13 14 15 16 17 18 19 20 21 > >>
View [10|25|50] records per page
| 國立臺灣大學 |
2010 |
Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 -> Q11.23 by Array Comparative Genomic Hybridization
|
陳持平; 蘇怡寧; 陳樹人; 蔡輔仁; 徐金源; 李貞姫; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; HSU, CHIN-YUAN; LEE, CHEN-CHI; WANG, WAYSEEN |
| 國立臺灣大學 |
2010 |
Prenatal Diagnosis of Rhabdomyomas and Cerebral Tuberous Sclerosis by Magnetic Resonance Imaging in One Fetus of a Dizygotic Twin Pregnancy Associated with a Frameshift Mutation in the Tsc2 Gene
|
陳持平; 蘇怡寧; 張東曜; 劉育朋; 蔡輔仁; 陳銘仁; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHANG, TUNG-YAO; LIU, YU-PENG; TSAI, FUU-JEN; CHEN, MING-REN; WANG, WAYSEEN |
| 國立臺灣大學 |
2010 |
Rapid Genome-Wide Aneuploidy Diagnosis Using Uncultured Amniocytes and Array Comparative Genomic Hybridization in Pregnancy with Abnormal Ultrasound Findings Detected in Late Second and Third Trimesters
|
陳持平; 蘇怡寧; 蔡輔仁; 陳樹人; 徐金源; 黃閔照; 王偉信; CHEN, CHIH-PING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; HSU, CHIN-YUAN; HUANG, MING-CHAO; 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
|
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
|
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 |
| 亞洲大學 |
2009-12 |
Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis
|
陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Wu, Pei-Chen;Lee, Chen-Chi;Chiang, Shu-Shien;Wang, Wayseen |
| 亞洲大學 |
2009-12 |
Limb-body wall complex in one fetus of a dizygotic twin pregnancy obtained by egg donation, in vitro fertilization and embryo transfer: prenatal diagnosis and literature review
|
陳持平;Chen, Chih-Ping;Lee, Maw-Shuan;Tsai, Fuu-Jen;Huang, Ming-Chao;Chern, Schu-Rern;Wang, Wayseen |
| 亞洲大學 |
2009-12 |
Prenatal diagnosis of a 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect by array comparative genomic hybridization
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chang, Tung-Yao;Chern, Schu-Rern;Tsai, Fuu-Jen;Hwang, Jonathan Kwei;Wang, Wayseen |
| 亞洲大學 |
2009-12 |
Prenatal diagnosis of monosomy 17p (17p13.3->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly and Miller-Dieker lissencephaly syndrome in a fetus
|
;Lin, Chin-Yi;陳持平;Chen, Chih-Ping;Liau, Chiung-Ling;Su, Pen-Hua;Tsao, Teng-Fu;Chang, Tung-Yao;Wang, Wayseen |
| 亞洲大學 |
2009-12 |
Prenatal diagnosis of terminal 2q deletion and distal 15q duplication by array comparative genomic hybridization using uncultured amniocytes
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Tsai, Fuu-Jen;Lin, Hung-Hung;Chern, Schu-Rern;Lee, Meng-Shan;Hwang, Jonathan Kwei;Chen, Teresa Hsiao-Tien;Wang, Wayseen |
Showing items 166-175 of 201 (21 Page(s) Totally)
<< < 12 13 14 15 16 17 18 19 20 21 > >>
View [10|25|50] records per page
|
