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"lin hung hung"
Showing items 1-11 of 11 (1 Page(s) Totally)
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| 亞洲大學 |
2010-12 |
Prenatal diagnosis of partial monosomy 1q (1q42.3->qter) associated with hydrocephalus and corpus callosum agenesis
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Lin, Hung-Hung;Wu, Pei-Chen;Lee, Chen-Chi;Pan, Chen-Wen;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 |
2010-02 |
Prenatal diagnosis of X-linked myotubular myopathy
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陳持平;Chen, Chih-Ping;Lin, Shuan-Pei;Chern, Schu-Rern;Tsai, Fuu-Jen;Wang, Tao-Yeuan;Lin, Hung-Hung;Wang, Wayseen |
| 國立臺灣大學 |
2010 |
Detection and Comparison of Cytomegalovirus DNA Levels 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; 蘇怡寧; 陳樹人; 王道遠; 蔡輔仁; 林虹宏; 吳佩臻; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; WANG, TAO-YEUAN; TSAI, FUU-JEN; LIN, HUNG-HUNG; WU, PEI-CHEN; 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 |
2009-09 |
Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review
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陳持平;Chen, Chih-Ping;Liu, Yu-Peng;Tsai, Fuu-Jen;Chen, Chen-Yu;Lin, Hung-Hung;Wu, Pei-Chen;Wang, Wayseen |
| 亞洲大學 |
2009-09 |
Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Lin, Hung-Hung;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2009-03 |
PRENATAL DIAGNOSIS OF 46,XX,DER(13;21)(Q10;Q10),+21 AND TRANSIENT ABNORMAL MYELOPOIESIS IN A FETUS WITH HEPATOSPLENOMEGALY AND SPONTANEOUS RESOLUTION OF FETAL ASCITES
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陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Chern, Schu-Rern;Chang, Tung-Yao;Hsu, Chin-Yuan;Lin, Hung-Hung;Wang, Wayseen |
| 國立臺灣大學 |
2009 |
Terminal 2q Deletion and Distal 15q Duplication: Prenatal Diagnosis by Array Comparative Genomic Hybridization Using Uncultured Amniocytes
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陳持平; 蘇怡寧; 蔡輔仁; 林虹宏; 陳樹人; 李孟珊; 王偉信; CHEN, CHIH-PING; SU, YI-NING; TSAI, FUU-JEN; LIN, HUNG-HUNG; CHERN, SCHU-RERN; LEE, MENG-SHAN; WANG, WAYSEEN |
| 亞洲大學 |
2008-12 |
LIMB-BODY WALL COMPLEX WITH CRANIOFACIAL DEFECTS AFTER OVARIAN STIMULATION
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陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Chen, Chen-Yu;Lin, Hung-Hung;Wang, Wayseen |
| 亞洲大學 |
2008-03 |
CONCOMITANT OMPHALOCELE AND ANENCEPHALY ASSOCIATED WITH TRISOMY 18 AND ARTHROGRYPOSIS DIAGNOSED IN EARLY PREGNANCY
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陳持平;Chen, Chih-Ping;Chang, Tung-Yao;Lin, Hung-Hung;Chern, Schu-Rern;Wang, Wayseen |
Showing items 1-11 of 11 (1 Page(s) Totally)
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