English  |  正體中文  |  简体中文  |  Total items :2856704  
Visitors :  53707825    Online Users :  921
Project Commissioned by the Ministry of Education
Project Executed by National Taiwan University Library
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
About TAIR

Browse By

News

Copyright

Related Links

Jump to: [ Chinese Items ] [ 0-9 ] [ A B C D E F G H I J K L M N O P Q R S T U V W X Y Z ]
or enter the first few letters:   

Showing items 682971-683020 of 2349128  (46983 Page(s) Totally)
<< < 13655 13656 13657 13658 13659 13660 13661 13662 13663 13664 > >>
View [10|25|50] records per page

Institution Date Title Author
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.
中國醫藥大學 2005 Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis Chen, CP; Chern, SR; Chen, LF; Chen, WL; Wang, W
中國醫藥大學 2006 Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus. 陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Chern SR,); (Lee CC,); (Chen LF,); (Wang W.)
亞洲大學 2016-12 Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome 陳持平;Chen, Chih-Ping;*;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學 2017-12 Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome 陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Lee, Chen-Chi;Wang, Wayseen
亞洲大學 2016-12 Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome 陳持平;Chen, Chih-Ping;*;Hung, Fang-Yu;Hung, Fang-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Le, Meng-Shan;Lee, Meng-Shan;Ya, Chien-Wen;Yang, Chien-Wen
亞洲大學 2016-04 Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome Chen)*, 陳持平(Chih-Ping;Ko), Tsang-Ming K(Tsang-Ming;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(Shin-Wen;Chen), Li-Feng Chen(Li-Feng;Yang), Chien-Wen Ya(Chien-Wen;Wang), Wayseen Wang(Wayseen
亞洲大學 2016-04 Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome 陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學 2016-04 Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome Wang;, 陳持平;Chih-Ping Chen;*;Tsang-Ming K;Tsang-Ming Ko;Schu-Rern Ch;Schu-Rern Chern;Peih-Shan Wu;Peih-Shan Wu;Yen-Ni Chen;Yen-Ni Chen;Shin-Wen Che;Shin-Wen Chen;Li-Feng Chen;Li-Feng Chen;Chien-Wen Ya;Chien-Wen Yang;Wayseen Wang;Wayseen
中國醫藥大學 2002 Prenatal diagnosis of lymphangiomas at unusual locations: report of three cases 何銘; 李建忠; 張穎宜; (戴金道); 蔡鴻德(Tsai,Horng-Der)
東海大學 2003-08 Prenatal diagnosis of Machado-Joseph disease/ Spinocerebellar Ataxia Type 3 in Taiwan: early detection of expanded ataxin-3. 謝明麗; Tsai, Hui-Fang; Liu, Chin-San; Chen, Gin-Den; Lin, Mei-Ling; Li, Chuan; Chen, Yi-Yun; Wang, Bao-Tyan; Hsieh, Mingli
中山醫學大學 2016 Prenatal diagnosis of Machado-Joseph disease/Spinocerebellar Ataxia Type 3 in Taiwan: early detection of expanded ataxin-3 HF, Tsai; CS, Liu; GD, Chen; ML, Lin; Li, C; YY, Chen; BT, Wang; Hsieh, M
臺北醫學大學 2000 Prenatal diagnosis of meconium peritonitis in a twin pregnancy after intracytoplasmic sperm injection: A case report 黃建榮; Seow KM; Cheng WC; Yeh ML; Hwang JL; Tsai YL;
國立臺灣大學 1985 Prenatal Diagnosis of Meconium Pseudocyst with Atypical Ultrasonographic Findings:A Case Report 謝豐舟; Chen, H. Y.; 陳維昭; Hsieh, Fon-Jou; Chen, H. Y.; Chen, Wei-Jao
亞洲大學 2011-09 Prenatal diagnosis of microvillus inclusion disease 陳持平;Chen, Chih-Ping
中國醫藥大學 2011-09 Prenatal diagnosis of microvillus inclusion disease 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Schu-Rern Chern);(Pei-Chen Wu);(Wayseen Wang)
國立臺灣大學 1998 Prenatal Diagnosis of Monosomy 10q25 Associated with Single Umbilical Artery and Sex Reversal: Report of a Case 鍾宜珮; 華筱玲; 曾麗慧; 徐明洸; 李建南; 謝豐舟; CHUNG, YI-PEI; HWA, HSIAO-LIN; TSENG, LI-HUI; SHYU, MING-KWANG; LEE, CHIEN-NAN; HSIEH, FON-JOU
臺大學術典藏 2018-09-10T06:52:50Z Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal: Report of a case Chung, Y.-P. and Hwa, H.-L. and Tseng, L.-H. and Shyu, M.-K. and Lee, C.-N. and Shih, J.-C. and Hsieh, F.-J.; MING-KWANG SHYU; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏 2020-02-03T08:15:26Z Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal: Report of a case Hsieh F.-J.;Shih J.-C.;Lee C.-N.;Shyu M.-K.;Tseng L.-H.;HSIAO-LIN HWA;Chung Y.-P.; Chung Y.-P.; HSIAO-LIN HWA; Tseng L.-H.; Shyu M.-K.; Lee C.-N.; Shih J.-C.; Hsieh F.-J.
臺大學術典藏 2020-02-12T04:06:50Z Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal: Report of a case Hsieh F.-J.;Shih J.-C;CHIEN-NAN LEE;Shyu M.-K;Tseng L.-H;Hwa H.-L;Chung Y.-P; Chung Y.-P; Hwa H.-L; Tseng L.-H; Shyu M.-K; CHIEN-NAN LEE; Shih J.-C; Hsieh F.-J.
臺大學術典藏 2020-02-14T05:49:52Z Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal: Report of a case Chung Y.-P;Hwa H.-L;Tseng L.-H;Ming-Kwang Shyu;Lee C.-N;Shih J.-C;Hsieh F.-J.; Chung Y.-P; Hwa H.-L; Tseng L.-H; MING-KWANG SHYU; Lee C.-N; Shih J.-C; Hsieh F.-J.
臺大學術典藏 2021-02-04T06:05:29Z Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal: Report of a case Chung Y.-P.; Hwa H.-L.; Tseng L.-H.; Shyu M.-K.; CHIEN-NAN LEE; Shih J.-C.; Hsieh F.-J.
臺大學術典藏 2021-02-04T06:47:11Z Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal: Report of a case Chung Y.-P.; Hwa H.-L.; Tseng L.-H.; Shyu M.-K.; Lee C.-N.; JIN-CHUNG SHIH; Hsieh F.-J.
臺大學術典藏 2022-03-10T07:58:54Z Prenatal diagnosis of monosomy 10q25 associated with single umbilical artery and sex reversal: Report of a case Chung Y.-P.; Hwa H.-L.; LI-HUI TSENG; Shyu M.-K.; Lee C.-N.; Shih J.-C.; Hsieh F.-J.
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 Lin, CY (Lin, Chin-Yi); Chen, CP (Chen, Chih-Ping); Liau, CL (Liau, Chiung-Ling); Su, PH (Su, Pen-Hua); Tsao, TF (Tsao, Teng-Fu); Chang, TY (Chang, Tung-Yao); Wang, WS (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 ;Lin, Chin-Yi;陳持平;Chen, Chih-Ping;Liau, Chiung-Ling;Su, Pen-Hua;Tsao, Teng-Fu;Chang, Tung-Yao;Wang, Wayseen
中國醫藥大學 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 (Chin-Yi Lin); 陳持平(Chih-Ping Chen)*; (Chiung-Ling Liau); (Pen-Hua Su); (Teng-Fu Tsao); (Tung-Yao Chang); (Wayseen Wang)
亞洲大學 2009-09 PRENATAL DIAGNOSIS OF MOS45,X/46,X,+MAR IN A FETUS WITH NORMAL MALE EXTERNAL GENITALIA AND A LITERATURE REVIEW Chien, SC (Chien, Shu-Chin); Chen, CP (Chen, Chih-Ping); Lin, CC (Lin, Chyi-Chyang); Huang, LC (Huang, Li-Chia); Hsieh, CT (Hsieh, Cheng-Tiao); Tsai, FJ (Tsai, Fuu-Jen)
中國醫藥大學 2009-10 Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and literature review 簡淑錦(Shu-Chin Chien); (Chih-Ping Chen); 林齊強(Chyi-Chyang Lin); 黃莉佳(Li-Chia Huang); (Cheng-Tiao Hsieh); 蔡輔仁(Fuu-Jen Tsai)*
國立臺灣大學 2004 Prenatal Diagnosis of Mos46,X,Del(Y)(Q11.2)/45,X by Cytogenetic and Molecular Studies with Multiplex Str Analysis 華筱玲; 柯滄銘; 蘇怡寧; 曾麗慧; 謝豐舟; HWA, HSIAO-LIN; KO, TSANG-MING; SU, YI-NING; TSENG, LI-HUI; HSIEH, FON-JOU
國立臺灣大學 2004-02 Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis Hwa, HL; Ko, TM; Chang, YY; Huang, CH; Su, YN; Tseng, LH; Hsieh, FJ
臺大學術典藏 2018-09-10T04:42:48Z Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis Hwa, H.-L.;Ko, T.-M.;Chang, Y.-Y.;Huang, C.-H.;Su, Y.-N.;Tseng, L.-H.;Hsieh, F.-J.; LI-HUI TSENG; HSIAO-LIN HWA
臺大學術典藏 2020-02-03T08:15:23Z Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis Hsiao-Lin Hwa;Ko T.-M.;Chang Y.-Y.;Huang C.-H.;Su Y.-N.;Tseng L.-H.;Hsieh F.-J.; HSIAO-LIN HWA; Ko T.-M.; Chang Y.-Y.; Huang C.-H.; Su Y.-N.; Tseng L.-H.; Hsieh F.-J.
臺大學術典藏 2022-03-10T07:58:50Z Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis Hwa H.-L.; Ko T.-M.; Chang Y.-Y.; Huang C.-H.; Su Y.-N.; LI-HUI TSENG; Hsieh F.-J.
亞洲大學 2008-09 Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele Chen, CP (Chen, Chih-Ping); Chen, YJ (Chen, Yann-Jang); Chern, SR (Chern, Schu-Rern); Tsai, FJ (Tsai, Fuu-Jen); Lin, HH (Lin, Hung-Hung); Lee, CC (Lee, Chen-Chi); Wang, W (Wang, Wayseen)
中國醫藥大學 2008-09 Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele. 陳持平(Chih-Ping Chen)*; (Yann-Jang Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Chen-Chi Lee); (Wayseen Wang)
亞洲大學 2012-03 Prenatal diagnosis of mosaic ring chromosome 15 with abnormal maternal serum Down syndrome screening and Dandy- Walker malformation 陳持平;Chen, Chih-Ping
中國醫藥大學 2007-05 Prenatal diagnosis of mosaic ring chromosome 4 陳持平(Chih-Ping Chen)*; 徐金源(Chin-Yuan Hsu); 曾嶔元(Chin-Yuan Tzen); 李貞姬(Chen-Chi Lee); 陳文玲(Wen-Lin Chen); 陳麗鳳(Li-Feng Chen); 王偉信(Wayseen Wang)
亞洲大學 2016-06 Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay Chen)*, 陳持平(Chih-Ping;Chiang), Sheng Chiang(Sheng;Wang), Kung-Liahng(Kung-Liahng;Cho), Fu-Nan Cho(Fu-Nan;Chen), Ming Chen(Ming;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;(Shin-Wen Chen,);(Shun-Ping Chang,);Chen), Weu-Lin Chen(Weu-Lin;Wang), Wayseen Wang(Wayseen
亞洲大學 2016-06 Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay 陳持平;Chen, Chih-Ping;*;Chiang, Sheng;Chiang, Sheng;Kung-Liahng;Wang, Kung-Liahng;Cho, Fu-Nan;Cho, Fu-Nan;Chen, Ming;Chen, Ming;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Shin-Wen Chen;Shun-Ping Chang;Chen, Weu-Lin;Chen, Weu-Lin;Wang, Wayseen;Wang, Wayseen
亞洲大學 2016-06 Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay 陳持平;Chih-Ping Chen;*;Sheng Chiang;Sheng Chiang;Kung-Liahng;Kung-Liahng Wang;Fu-Nan Cho;Fu-Nan Cho;Ming Chen;Ming Chen;Schu-Rern Ch;Schu-Rern Chern;Peih-Shan Wu;Peih-Shan Wu;Yen-Ni Chen;Yen-Ni Chen;, ;Shin-Wen Chen,;,;Shun-Ping Chang,;Weu-Lin Chen;Weu-Lin Chen;Wayseen Wang;Wayseen Wang;;
臺大學術典藏 2018-09-10T15:38:52Z Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay Chen, C.-P.;Chiang, S.;Wang, K.-L.;Cho, F.-N.;Chen, M.;Chern, S.-R.;Wu, P.-S.;Chen, Y.-N.;Chen, S.-W.;Chang, S.-P.;Chen, W.-L.;Wang, W.; MING CHEN
中國醫藥大學 2003 Prenatal diagnosis of mosaic tetrasomy 10p associated with megacisterna magna, echogenic focus of left ventricle, umbilical cord cysts and distal arthrogryposis Wu, YC; Yu, MT; Chen, LC; Chen, CL; Yang, ML
中國醫藥大學 2012-12 Prenatal diagnosis of mosaic tetrasomy 18p 陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Yi-Ning Su);(Schu-Rern Chern);(Jun-Wei Su);(Yu-Ting Chen);(Dai-Dyi Town);(Wayseen Wang)
亞洲大學 201309 Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth 陳持平;Chen, Chih-Ping;Ch, Shing-Jyh;Chang, Shing-Jyh;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Wang, Wayseen;Wang, Wayseen
臺大學術典藏 2021-02-04T06:46:55Z Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin Chen C.-P.;Jin-Chung Shih;Chern S.-R.;Lee C.-C.;Wang W.; Chen C.-P.; JIN-CHUNG SHIH; Chern S.-R.; Lee C.-C.; Wang W.

Showing items 682971-683020 of 2349128  (46983 Page(s) Totally)
<< < 13655 13656 13657 13658 13659 13660 13661 13662 13663 13664 > >>
View [10|25|50] records per page