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"陳持平"的相關文件
顯示項目 261-270 / 339 (共34頁)
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| 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 |
Second-Trimester Maternal Serum Quadruple Test for down Syndrome Screening : A Taiwanese Population-Based Study
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蕭勝文; 林芯伃; 林佳慧; 蘇怡寧; 鄭博仁; 李建南; 陳持平; SHAW, SHENG-WEN; LIN, SHIN-YU; LIN, CHIA-HUI; SU, YI-NING; CHENG, PO-JEN; LEE, CHIEN-NAN; CHEN, CHIH-PING |
| 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 |
| 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 |
| 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
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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
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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
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;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
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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 |
| 亞洲大學 |
2009-12 |
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (III)
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陳持平;Chen, Chih-Ping |
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