| 國立臺灣大學 |
1994 |
Prenatal diagnosis of congenital rubella infection from maternal rubella in Taiwan
|
華筱玲; 徐明洸; 李建南; 吳志正; 高全良; 謝豐舟; HWA, HSIAO-LIN; SHYU, MING-KWANG; LEE, CHIEN-NAN; WU, CHIH-CHENG; KAO, CHUAN-LIANG; HSIEH, FON-JOU |
| 臺大學術典藏 |
2018-09-10T04:42:48Z |
Prenatal diagnosis of congenital rubella infection from maternal rubella in Taiwan
|
Hwa, H.-L. and Shyu, M.-K. and Lee, C.-N. and Wu, C.-C. and Kao, C.-L. and Hsieh, F.-J.; HSIAO-LIN HWA |
| 臺大學術典藏 |
2018-09-10T04:43:53Z |
Prenatal diagnosis of congenital rubella infection from maternal rubella in Taiwan
|
Hwa, H.-L. and Shyu, M.-K. and Lee, C.-N. and Wu, C.-C. and Kao, C.-L. and Hsieh, F.-J.; MING-KWANG SHYU |
| 臺大學術典藏 |
2021-02-04T06:47:08Z |
Prenatal diagnosis of conjoined twins with three-dimensional sonography at 13 weeks of gestation: Report of a case
|
Su Y.-C.;Liou Y.-S.;Jin-Chung Shih; Su Y.-C.; Liou Y.-S.; JIN-CHUNG SHIH |
| 臺大學術典藏 |
2022-04-27T02:14:41Z |
PRENATAL DIAGNOSIS OF CONJOINTED TWINS BY REAL-TIME SONOGRAPHY - A CASE STUDY.
|
Chen H.Y.; Hsieh F.J.; LIAN-HUA HUANG |
| 中國醫藥大學 |
2007-09 |
Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies
|
陳持平(Chih-Ping Chen)* |
| 國立成功大學 |
2003-06 |
Prenatal diagnosis of Dandy-Walker syndrome in early pregnancy presenting with increased nuchal translucency and generalized edema at 13 weeks of gestation
|
Chen, Sheng-Hsien; Lin, Mike Yan-Sheng; Chang, Fong-Ming |
| 中國醫藥大學 |
2013-12 |
Prenatal diagnosis of de novo cryptic microdeletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect
|
陳持平(Chih-Ping Chen)*;(Ming-Chao Huang);(Yi-Yung Chen);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Jun-Wei Su);(Wayseen Wang) |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis of de novo partial trisomy 13q (13q22 -> qter) and partial monosomy 8p (8p23.3 -> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart
|
Chen, CP; Chern, SR; Hsu, CY; Lee, CC; Lee, MS; Wang, WS |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency
|
Chen, CP; Chern, SR; Chang, TY; Chen, WL; Chen, LF; Wang, WS; Chen, HEC |
| 中國醫藥大學 |
2006 |
Prenatal diagnosis of de novo t(2;18;14) (q33.1;q12.2; q31.2),dup(5)(q34q34), del(7)(p21.1p21.1), and del(10) (q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements
|
陳持平(Chen CP,); (Chern SR,); (Lee CC,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Chen WL,); (Wang W.) |
| 亞洲大學 |
2011-09 |
Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene
|
陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2011-09 |
Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Yu-Ting Chen);(Wen-Lin Chen);(Lee James Hsu);(Wayseen Wang) |
| 國立臺灣大學 |
1984 |
Prenatal Diagnosis of Down's Syndrome with Matemal Balanced 15P/21G translocation and Paternal 47 XXY/46XY Mosaicism
|
莊壽洺; Ko, T. M.; Lee, T. Y.; Yu, T. K.; Chuang, Sou-Ming; Ko, T. M.; Lee, T. Y.; Yu, T. K. |
| 中國醫藥大學 |
1999 |
Prenatal diagnosis of dyssegmental dysplasia - A case report
|
Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, FJ; Tsai, CH |
| 中國醫藥大學 |
1999 |
Prenatal diagnosis of dyssegmental dysplasia - A case report
|
Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, FJ; Tsai, CH |
| 亞洲大學 |
2016-12 |
Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality
|
陳持平;Chen, Chih-Ping;*;Fu, Chung-Hu;Fu, Chung-Hu;Lin, Yi-Hui;Lin, Yi-Hui;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Wang, Wayseen;Wang, Wayseen |
| 國立成功大學 |
2005-02 |
Prenatal diagnosis of fetal acrania using three-dimensional ultrasound
|
Liu, I.-Feng; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Cheng, Yueh-Chin; Chang, Fong-Ming |
| 國立交通大學 |
2018-08-21T05:54:32Z |
Prenatal diagnosis of fetal aneuploidy and de novo copy number variation by isolating extravillus trophoblasts and nucleated fetal red blood cells from maternal circulation a proof of principle study using the automated Cell RevealTM platform based on nanostructure and microfluidics
|
Chen, Ming; Huang, Chung-Er; Chang, Frank Mau-Chung |
| 國立臺灣大學 |
1993 |
Prenatal Diagnosis of Fetal Atrial Flutter:A Case Report
|
Lin, U. F.; Lee, Chien-Nan; O., J. W.; 謝豐舟; 陳皙堯; Lin, U. F.; Lee, Chien-Nan; O., J. W.; Hsieh, Fon-Jou; Chen, Hsi-Yao |
| 亞洲大學 |
2013 |
Prenatal diagnosis of fetal congenital cystic adenomatoid malformation of the lung using three-dimensional ultrasound: Comparison between the 20th and 21st centuries
|
Tsai, HF;Tsai, HF;Cheng, YC;Cheng, YC;柯慧貞;jennyko;Huei-Chen Ko;Kang, L;Kang, L;Tsai, PY;Tsai, PY;Yu, CH;Yu, CH;Chang, CH;Chang, CH;Chang, FM;Chang, FM |
| 國立成功大學 |
2013-03 |
Prenatal diagnosis of fetal congenital cystic adenomatoid malformation of the lung using three-dimensional ultrasound: Comparison between the 20th and 21st centuries
|
Tsai, Hsing-Fen; Cheng, Yueh-Chin; Ko, Huei-Chen; Kang, Lin; Tsai, Pei-Yin; Yu, Chen-Hsiang; Chang, Chiung-Hsin; Chang, Fong-Ming |
| 國立成功大學 |
2021-04~2021-06 |
Prenatal Diagnosis of Fetal Congenital Mesoblastic Nephroma and Neonatal Follow-up
|
Lin;Li-Chan;Cheng;Yueh-Chin;Chang;Chiung-Hsin |
| 國立成功大學 |
2013-06 |
Prenatal diagnosis of fetal gastroschisis using three-dimensional ultrasound: Comparison between the 20th and 21st centuries
|
Tsai, Hsing-Fen; Cheng, Yueh-Chin; Ko, Huei-Chen; Kang, Lin; Tsai, Pei-Yin; Yu, Chen-Hsiang; Chang, Chiung-Hsin; Chang, Fong-Ming |
| 中國醫藥大學 |
2011-01 |
Prenatal diagnosis of fetal hepatoblastoma with a good neonatal outcome: case report and narrative literature review
|
黃莉佳(Li-Chia Huang)*; 何銘(Ming- Ho); 張維君(Wei-Chun Chang); 陳慧毅(Huey-Yi Chen); 洪耀欽(Yao-Ching Hung); 邱燦宏(Tsan-Hung Chiu) |
| 國立成功大學 |
2012-12 |
Prenatal diagnosis of fetal multicystic dysplastic kidney in the era of three-dimensional ultrasound: 10-year experience
|
Hsu, PY (Hsu, Pei-Yang); Yu, CH (Yu, Chen-Hsiang); Lin, K (Lin, Kang); Cheng, YC (Cheng, Yueh-Chin); Chang, CH (Chang, Chiung-Hsin); Chang, FM (Chang, Fong-Ming) |
| 國立成功大學 |
2002-07 |
Prenatal diagnosis of fetal multicystic dysplastic kidney with two-dimensional and three-dimensional ultrasound
|
Chang, Ling-Wei; Chang, Fong-Ming; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Cheng, Yueh-Chin; Chen, Hsi-Yao |
| 國立臺灣大學 |
1991 |
Prenatal Diagnosis of Fetal Nuchal Cord Coiling with Color Doppler Imaging:A Case Report
|
Lee, Chien-Nan; 謝豐舟; 何弘能; Tsai, Yieh-Loong; 柯滄銘; 陳皙堯; Kao, Miao-Lin; Lee, Chien-Nan; 謝豐舟; 何弘能; Tsai, Yieh-Loong; 柯滄銘; Chen, Hsi-Yao; Kao, Miao-Lin |
| 亞洲大學 |
201407 |
Prenatal diagnosis of fetal omphalocele by ultrasound: a comparison of two centuries
|
Anonymous |
| 國立成功大學 |
2013-06 |
Prenatal diagnosis of fetal omphalocele by ultrasound: A comparison of two centuries
|
Liang, Yu-Ling; Kang, Lin; Tsai, Pei-Ying; Cheng, Yueh-Chin; Ko, Huei-Chen; Chang, Chiung-Hsin; Chang, Fong-Ming |
| 中國醫藥大學 |
2007-10 |
Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1
|
陳持平(Chih-Ping Chen)* |
| 臺大學術典藏 |
2022-03-10T07:59:00Z |
Prenatal diagnosis of Hb H disease due to compound heterozygosity for South?East Asian deletion and Hb constant spring by polymerase chain reaction
|
Ko T.?M.; LI-HUI TSENG; Hsieh F.?J.; Lee T.?Y. |
| 國立臺灣大學 |
1993 |
Prenatal Diagnosis of HbH Disease Due to Compound Heterozygosity for Southeast Asian Deletion and Hb Constant Spring by Polymerase Chain Reaction
|
柯滄銘; Tseng, Li-Hui; 謝豐舟; Lee, Tzu-Yao; Ko, Tsang-Ming; Tseng, Li-Hui; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 國立臺灣大學 |
1990 |
Prenatal Diagnosis of Hemophilia A by DNA Analysis on Chorionic Villi
|
柯滄銘; Shen, Ming-Ching; 謝豐舟; Lee, Tzu-Yao; Ko, Tsang-Ming; Shen, Ming-Ching; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 國立成功大學 |
2003-02 |
Prenatal diagnosis of holoprosencephaly in two fetuses with der (7)t(1;7)(q32;q32)pat inherited from the father with double translocations
|
Chuang, Louise; Kuo, Pao-Lin; Yang, Hsiao-Bai; Chien, Chung-Ho; Chen, Pei-Yi; Chang, Chiung-Hsin; Chang, Fong-Ming |
| 國立臺灣大學 |
1988 |
Prenatal Diagnosis of Homozygous Alpha Thalassemia-1 and Hb Disease by Analysis of Alpha Globin Gene in Amniocytes or Chorionic Villi
|
Ko, T. M.; 謝豐舟; 李鎡堯; Ko, T. M.; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 國立臺灣大學 |
1990 |
Prenatal Diagnosis of Homozygous Beta-Thalassemia by Chorionic Villus Sampling and DNA Polymorphism Study
|
Chen, Tao-Shih; Wang, Shin-Tai; 柯滄銘; Chen, Tao-Shih; Wang, Shin-Tai; Ko, Tsang-Ming |
| 亞洲大學 |
2018-02 |
Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia
|
陳持平;Chen, Chih-Ping;*;Cha, Tung-Yao;Chang, Tung-Yao;Lin, Tan-Wei;Lin, Tan-Wei;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2014-03 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Che, Shee-Uan;Chen, Shee-Uan;Cha, Tung-Yao;Chang, Tung-Yao;Wu, Pei-Chen;Wu, Pei-Chen;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Kuo, Yu-Ling;Kuo, Yu-Ling;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2014-03 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET
|
Chih-Ping Chen;Yi-Ning Su;Shee-Uan Chen;Tung-Yao Chang;Pei-Chen Wu;Schu-Rern Chern;Peih-Shan Wu;Yu-Ling Kuo;Wayseen Wang |
| 中國醫藥大學 |
2014-03 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Shee-Uan Chen);(Tung-Yao Chang);(Pei-Chen Wu);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ling Kuo);(Wayseen Wang) |
| 臺北醫學大學 |
2014 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer
|
Chen, Chih-Ping;Su, Yi-Ning;Chen, Shee-Uan;Chang, Tung-Yao;Wu, Pei-Chen;Chern, Schu-Rern;Wu, Peih-Shan;Kuo, Yu-Ling;Wang, Wayseen |
| 臺大學術典藏 |
2020-02-06T06:49:57Z |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived byintracytoplasmic sperm injection and invitro fertilization andembryo transfer
|
Chen C.-P;Su Y.-N;Shee-Uan Chen;Chang T.-Y;Wu P.-C;Chern S.-R;Wu P.-S;Kuo Y.-L;Wang W.; Chen C.-P; Su Y.-N; SHEE-UAN CHEN; Chang T.-Y; Wu P.-C; Chern S.-R; Wu P.-S; Kuo Y.-L; Wang W. |
| 國立成功大學 |
1999-11 |
Prenatal diagnosis of Joubert syndrome complicated with encephalocele using two-dimensional and three-dimensional ultrasound
|
Wang, P; Chang, Fong-Ming; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Jung, Y. C.; Huang, C. C. |
| 國立臺灣大學 |
1993 |
Prenatal Diagnosis of Left-Sided Congenital Diaphragmatic Hernia with Hepatic Protrusion Demonstrated by Color Doppler Ultrasound:a Case Report
|
Jehng, Chin-Huoo; 謝豐舟; Lai, Ming-Chin; Yang, Li-Fang; Jehng, Chin-Huoo; Hsieh, Fon-Jou; Lai, Ming-Chin; Yang, Li-Fang |
| 國立成功大學 |
2003-06 |
Prenatal diagnosis of limb-body wall complex in early pregnancy using three-dimensional ultrasound
|
Liu, I-Feng; Yu, Chiung-Hsing; Chang, Chiung-Hsing; Chang, Fong-Ming |
| 臺大學術典藏 |
2021-02-04T06:47:02Z |
Prenatal diagnosis of limb-body wall complex using two- and three-dimensional ultrasound [3]
|
Chen C.-P.;Jin-Chung Shih;Chan Y.-J.; Chen C.-P.; JIN-CHUNG SHIH; Chan Y.-J. |
| 亞洲大學 |
2011-09 |
Prenatal diagnosis of limb-body wall complex with craniofacial defects
|
陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2011-09 |
Prenatal diagnosis of limb-body wall complex with craniofacial defects
|
陳持平(Chih-Ping Chen)*;(Yi-Yung Chen);(Jun-Wei Su);(Wayseen Wang) |
| 臺大學術典藏 |
2021-03-02T06:21:25Z |
Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome
|
Chen C.-P.;Shin-Yu Lin;Chern S.-R.;Wu P.-S.;Chen S.-W.;Wu F.-T.;Town D.-D.;Wang W.; Chen C.-P.; SHIN-YU LIN; Chern S.-R.; Wu P.-S.; Chen S.-W.; Wu F.-T.; Town D.-D.; Wang W. |
