| 中國醫藥大學 |
2009-09 |
Prenatal diagnosis of and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly
|
陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Kevin Ko); (Wayseen Wang) |
| 中國醫藥大學 |
2009-09 |
Prenatal diagnosis of and molecular analysis of trisomy 13 mosaicism
|
陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Chen-Wen Pan); (Wayseen Wang) |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3->q23.3) associated with abnormal maternal serum biochemistry
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis of and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3->q23.3) associated with abnormal maternal serum biochemistry
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Shuan-Pei Lin);(Schu-Rern Chern);(Jun-Wei Su);(Yu-Ting Chen);(Meng-Shan Lee);(Wayseen Wang) |
| 中國醫藥大學 |
1998 |
Prenatal diagnosis of Apert syndrome
|
Chang, CC; Tsai, FJ; Tsai, HD; Tsai, CH; Hsieh, YY; Lee, CC; Yang, TC; Wu, JY |
| 中國醫藥大學 |
2007-06 |
Prenatal diagnosis of atypical facial clefting should alert amniotic band syndrome and prompt a search for associated amniotic bands and other structural anomalies
|
陳持平(Chih-Ping Chen)* |
| 臺大學術典藏 |
2021-02-04T06:47:06Z |
Prenatal diagnosis of bilateral ventriculomegaly and an enlarged cisterna magna in a fetus with partial trisomy 9 and partial trisomy 21 [1]
|
Chen C.-P.;Jin-Chung Shih; Chen C.-P.; JIN-CHUNG SHIH |
| 國立臺灣大學 |
2003 |
Prenatal Diagnosis of Cephalothoracopagus Janiceps Disymmetros Using Three-Dimensional Power Doppler Ultrasound and Magnetic Resonance Imaging
|
施景中; SHIH, JIN-CHUNG |
| 臺大學術典藏 |
2018-09-10T04:32:16Z |
Prenatal diagnosis of cephalothoracopagus janiceps disymmetros using three-dimensional power Doppler ultrasound and magnetic resonance imaging
|
Chen, C.-P. and Shih, J.-C. and Shih, S.-L. and Huang, J.-K. and Huang, J.-P. and Lin, Y.-H. and Wang, W.; JIN-CHUNG SHIH |
| 臺大學術典藏 |
2021-02-04T06:46:55Z |
Prenatal diagnosis of cephalothoracopagus janiceps disymmetros using three-dimensional power Doppler ultrasound and magnetic resonance imaging
|
Chen C.-P.;Jin-Chung Shih;Shih S.-L.;Huang J.-K.;Huang J.-P.;Lin Y.-H.;Wang W.; Chen C.-P.; JIN-CHUNG SHIH; Shih S.-L.; Huang J.-K.; Huang J.-P.; Lin Y.-H.; Wang W. |
| 亞洲大學 |
2011-06 |
Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene
|
陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2011-06 |
Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Chin-Yuan Hsu);(Ming-Ren Chen);(Yu-Peng Liu);(Pei-Chen Wu);(Wayseen Wang) |
| 國立臺灣大學 |
1990 |
Prenatal Diagnosis of Chinese Homozygous Alpha-Thalassemia 1 and Haemoglobin H Disease by Analysis of Alpha-and Pseudo-Zeta-Globin Genes in Chorionic Villi and Amniocytes
|
柯滄銘; 謝豐舟; Lee, Tzu-Yao; Ko, Tsang-Ming; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 國立臺灣大學 |
1989 |
Prenatal Diagnosis of Chinese Homozyous a-Thalassaemia 1 and Haemoglobin H Disease by Anbalysis of a-and-Globin Genes in Chorionic Villi and Amniocytes
|
Ko, T. M.; 謝豐舟; 李鎡堯; Ko, T. M.; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 中國醫藥大學 |
2015-12 |
Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly
|
陳持平(Chih-Ping Chen)*;(Cheng-Ran Peng);(Tung-Yao Chang);(Wan-Yuo Guo);(Yen-Ni Chen);(Peih-Shan Wu);(Dai-Dyi Town);(Wayseen Wang) |
| 國立臺灣大學 |
1990 |
Prenatal Diagnosis of Chromosome Mosaic 46, XY/46, XY, i(17q) by Amniocentesis:Report of One Case
|
Perng, Bao-Chin; 柯滄銘; 謝豐舟; Lee, Tzu-Yao; Perng, Bao-Chin; Ko, Tsang-Ming; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 國立臺灣大學 |
1990 |
PRENATAL DIAGNOSIS OF CHROMOSOME MOSAIC 46,XY/46,XY,i(17q)BY AMNIOCENTESIS - REPORT OF ONE CASE
|
柯滄銘; 謝豐舟; 李鎡堯; PERNG, BAO-CHIN; KO, TSANG-MING; HSIEH, FON-JOU; LEE, TZU-YAO |
| 國立成功大學 |
2001-08 |
Prenatal diagnosis of cleft palate by three-dimensional ultrasound
|
Chen, Min-Long; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Cheng, Yueh-Chin; Chang, Fong-Ming |
| 中國醫藥大學 |
2014-06-21 |
Prenatal diagnosis of coarctation of the aorta
|
裘品筠;彭義欽;莊子瑤;張正成(Jeng-Sheng Chang);裘品筠;張正成(Jeng-Sheng Chang) |
| 臺大學術典藏 |
2020-03-04T08:52:28Z |
Prenatal diagnosis of coarctation of the aorta with ventricular septal defect: A case report
|
Huang Y.-L.;Hsu K.-H.;Chuluunbaatar E.;Wen T.-M.;Li Y.-Y.;Chen M.-R.;Chung-I Chang;Chang T.-Y.; Huang Y.-L.; Hsu K.-H.; Chuluunbaatar E.; Wen T.-M.; Li Y.-Y.; Chen M.-R.; CHUNG-I CHANG; Chang T.-Y. |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes
|
Chen, CP; Chen, CY; Lin, CY; Shaw, SW; Wang, WS; Tzen, CY |
| 亞洲大學 |
2020-01-20 |
Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects
|
Ch, Chih-Ping;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Che, Shin-Wen;Chen, Shin-Wen;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Wu, Fang-Tzu;Wu, Fang-Tzu;Chen, Wen-Lin;Chen, Wen-Lin;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen |
| 中國醫藥大學 |
2007.05 |
Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution.
|
陳持平(Chen CP)*; 劉玉鵬(Liu YP); 簡淑錦(Shu-Chin Chien); 王偉信(Wang W) |
| 中國醫藥大學 |
2008-05 |
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand foot malformation associated with partial monosomy 4p (4p16.1->pter) and partial trisomy 10q (10q25.1->qter)
|
陳持平(Chih-Ping Chen); (Yann-Jang Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Tung-Yao Chang); (Chen-Chi Lee); (Dai-Dyi Town); (Meng-Shan Lee); (Wayseen Wang) |
| 亞洲大學 |
2008-05 |
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1 -> pter) and partial trisomy 10q (10q25.1 -> qter)
|
Chen, CP (Chen, Chih-Ping); Chen, YJ (Chen, Yann-Jang); Chern, SR (Chern, Schu-Rern); Tsai, FJ (Tsai, Fuu-Jen); Chang, TY (Chang, Tung-Yao); Lee, CC (Lee, Chen-Chi); Town, DD (Town, Dai-Dyi); Lee, MS (Lee, Meng-Shan); Wang, W (Wang, Wayseen) |
