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Showing items 683001-683025 of 2349128 (93966 Page(s) Totally)
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| 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
|
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
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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
|
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
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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.
|
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
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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
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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
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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. |
Showing items 683001-683025 of 2349128 (93966 Page(s) Totally)
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