|
|
Taiwan Academic Institutional Repository >
Browse by Author
|
"陳持平"
Showing items 301-310 of 339 (34 Page(s) Totally) << < 25 26 27 28 29 30 31 32 33 34 > >> View [10|25|50] records per page
| 亞洲大學 |
2008-06 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTS (III)
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2008-06 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTS (IV)
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2008-03 |
CONCOMITANT OMPHALOCELE AND ANENCEPHALY ASSOCIATED WITH TRISOMY 18 AND ARTHROGRYPOSIS DIAGNOSED IN EARLY PREGNANCY
|
陳持平;Chen, Chih-Ping;Chang, Tung-Yao;Lin, Hung-Hung;Chern, Schu-Rern;Wang, Wayseen |
| 亞洲大學 |
2008-03 |
PRENATAL VISUALIZATION OF CEBOCEPHALY WITH A PROMINENT NOSE IN A SECOND-TRIMESTER FETUS WITH ALOBAR HOLOPROSENCEPHALY AND TRISOMY 13
|
陳持平;Chen, Chih-Ping;Shih, Jin-Chung;Tzen, Chin-Yuan;Chern, Schu-Rern;Lin, Chen-Ju;Wang, Wayseen |
| 亞洲大學 |
2008-03 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTS (I)
|
陳持平;Chen, Chih-Ping |
| 亞洲大學 |
2008-03 |
SYNDROMES, DISORDERS AND MATERNAL RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTS (II)
|
陳持平;Chen, Chih-Ping |
| 國立臺灣大學 |
2008 |
Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis
|
Hung, Chia-Cheng; Lee, Chien-Nan; Chang, Chien-Hui; Jong, Yuh-Jyh; Chen, Chih-Ping; Hsieh, Wu-Shiun; Su, Yi-Ning; Lin, Win-Li; 洪加政; 李建南; 張千慧; 鐘育志; 陳持平; 謝武勳; 蘇怡寧; 林文澧 |
| 國立臺灣大學 |
2008 |
First- and Second-Trim Ester down Syndrome Screening: Current Strategies and Clinical Guidelines
|
蕭勝文; 徐振傑; 李建南; 蕭慶華; 陳持平; 謝燦堂; 鄭博仁; SHAW, SHENG-WEN; HSU, JENN-J; LEE, CHIEN- NAN; HSIAO, CHING-HUA; CHEN, CHIH-PING; HSIEH, T'SANG-T'ANG; CHENG, PO-JEN |
| 國立臺灣大學 |
2008 |
Genetic Analysis of Mucopolysaccharidosis Type Vi in Taiwanese Patients
|
林瑋德; 林炫沛; 王仲興; 胡務亮; 莊志光; 林秀娟; 陳持平; 蔡輔仁; LIN, WEI-DE; LIN, SHUAN-PEI; WANG, CHUNG- HSING; HWU, WUH-LIANG; CHUANG, CHIH-KUANG; LIN, SHIO-JEAN; CHEN, CHIH-PING; TSAI, FUU- JEN |
| 國立臺灣大學 |
2008 |
Craniosynostosis and Congenital Tracheal Anomalies in an Infant with Pfeiffer Syndrome Carrying the W290c Fgfr2 Mutation
|
陳持平; 林炫沛; 蘇怡寧; 蔡輔仁; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; SU, YI-NING; TSAI, FUU-JEN; WANG, WAYSEEN |
Showing items 301-310 of 339 (34 Page(s) Totally) << < 25 26 27 28 29 30 31 32 33 34 > >> View [10|25|50] records per page
|