| 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. |
