臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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顯示項目 682951-683000 / 2349128 (共46983頁)
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機構	日期	題名	作者
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.
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

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	造訪人次 : 53709493 線上人數 : 1955 教育部委託研究計畫計畫執行:國立臺灣大學圖書館