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Showing items 682991-683015 of 2349128 (93966 Page(s) Totally) << < 27315 27316 27317 27318 27319 27320 27321 27322 27323 27324 > >> View [10|25|50] records per page
| 國立臺灣大學 |
1998 |
Prenatal Diagnosis of Monosomy 10q25 Associated with Single Umbilical Artery and Sex Reversal: Report of a Case
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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
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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
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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
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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
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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
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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
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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
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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
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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
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;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
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(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
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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
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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
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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
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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
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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
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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
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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
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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.
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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
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陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2007-05 |
Prenatal diagnosis of mosaic ring chromosome 4
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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
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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
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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
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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;; |
Showing items 682991-683015 of 2349128 (93966 Page(s) Totally) << < 27315 27316 27317 27318 27319 27320 27321 27322 27323 27324 > >> View [10|25|50] records per page
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