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显示项目 682896-682905 / 2349128 (共234913页)
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| 國立臺灣大學 |
1990 |
Prenatal Diagnosis of Chromosome Mosaic 46, XY/46, XY, i(17q) by Amniocentesis:Report of One Case
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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
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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
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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
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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
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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
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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
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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.
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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)
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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)
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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) |
显示项目 682896-682905 / 2349128 (共234913页)
<< < 68285 68286 68287 68288 68289 68290 68291 68292 68293 68294 > >>
每页显示[10|25|50]项目
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