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 |
國立臺灣大學 |
2004 |
Prenatal Diagnosis of Mosaic Trisomy 16 Associated with Congenital Diaphragmatic Hernia and Elevated Maternal Serum Alpha-Fetoprotein and Human Chorionic Gonadotrophin
|
陳持平; 施景中; 陳樹人; 李貞姬; 王偉信; CHEN, CHIH-PING; SHIH, JIN-CHUNG; CHERN, SCHU-RERN; LEE, CHEN-CHI; 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. |
亞洲大學 |
201309 |
Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly and facial dysmorphism
|
陳持平;Chen, Chih-Ping;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Lee, Chen-Chi;Lee, Chen-Chi;Chen, Li-Feng;Li-Feng Chen, ;Wang, Wayseen;Wang, Wayseen |
亞洲大學 |
2011-09 |
Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction
|
陳持平;Chen, Chih-Ping |
中國醫藥大學 |
2011-09 |
Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Shin-Yu Lin);(Schu-Rern Chern);(Yu-Ting Chen);(Meng-Shan Lee);(Wayseen Wang) |
臺大學術典藏 |
2020-02-10T06:49:21Z |
Prenatal diagnosis of mosaic trisomy 2: Discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction
|
Chen C.-P;Su Y.-N;Shin-Yu Lin;Chern S.-R;Chen Y.-T;Lee M.-S;Wang W.; Chen C.-P; Su Y.-N; SHIN-YU LIN; Chern S.-R; Chen Y.-T; Lee M.-S; Wang W. |
亞洲大學 |
2020-01-20 |
Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum
|
Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wang, Wayseen; Ch, Chih-Ping; Chen, Chih-Ping; Hs, Chin-Yuan; Hsu, Chin-Yuan |
亞洲大學 |
2011-09 |
Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review
|
陳持平;Chen, Chih-Ping |
國立臺灣大學 |
2011 |
Prenatal Diagnosis of Mosaic Trisomy 8: Clinical Report and Literature Review
|
陳持平; 陳明; 潘怡如; 蘇怡寧; 陳樹人; 蔡輔仁; 王偉信; CHEN, CHIH-PING; CHEN, MING; PAN, YI-JU; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN |
中國醫藥大學 |
2011-09 |
Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review
|
陳持平(Chih-Ping Chen)*;(Ming Chen);(Yi-Ju Pan);(Yi-Ning Su);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Yu-Ting Chen);(Wayseen Wang) |
臺大學術典藏 |
2018-09-10T08:50:12Z |
Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review
|
Chen, Y.-T.;Wang, W.;Chen, Chih-Ping;Chen, Ming;Pan, Yi-Ju;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Wang, Wayseen; CHEN, CHIH-PING;CHEN, MING;PAN, YI-JU;SU, YI-NING;CHERN, SCHU-RERN;TSAI, FUU-JEN;WANG, WAYSEEN; 陳持平;陳明;潘怡如;蘇怡寧;陳樹人;蔡輔仁;王偉信; MING CHEN; CHEN, CHIH-PING; CHEN, MING; PAN, YI-JU; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WANG, WAYSEEN |