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Showing items 682826-682850 of 2349128 (93966 Page(s) Totally)
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| 臺大學術典藏 |
2020-02-03T08:15:26Z |
Prenatal diagnosis and perinatal outcome of facial clefts
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Pan Y.-J.; Shih J.-C.; Lee C.-N.; Shyu M.-K.; HSIAO-LIN HWA; Chen H.-Y.; Hsieh F.- J. |
| 臺大學術典藏 |
2020-02-12T04:06:51Z |
Prenatal diagnosis and perinatal outcome of facial clefts
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Hsieh F.- J.;Chen H.-Y;Hwa H.-L;Shyu M.-K;CHIEN-NAN LEE;Shih J.-C;Pan Y.-J; Pan Y.-J; Shih J.-C; CHIEN-NAN LEE; Shyu M.-K; Hwa H.-L; Chen H.-Y; Hsieh F.- J. |
| 國立臺灣大學 |
1987 |
Prenatal Diagnosis and Postnatal Management of Surgically Correctable Fatal Malformations
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Hsieh, F. J.; Lin, C. R.; 陳維昭; 陳秋江; Tsai, T. C.; Hsieh, F. J.; Lin, C. R.; Chen, Wei-Jao; Chen, Chiu-Chiang; Tsai, T. C. |
| 國立臺灣大學 |
1989 |
Prenatal Diagnosis and Postnatal Management of Surgically Correctable Fetal Malformations
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謝豐舟; 林啟瑞; 陳維昭; 陳秋江; 蔡崇璋; HSIEH, FON-JOU; LIN, CHII-RUAY; CHEN, WEI-JAO; CHEN, CHIU-CHIANG; TSAI, TSONG-CHANG |
| 臺大學術典藏 |
2018-09-10T04:05:34Z |
Prenatal diagnosis and treatment of fetal long QT syndrome: A case report
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Chang, I.-K. and Shyu, M.-K. and Lee, C.-N. and Kau, M.-L. and Ko, Y.-H. and Chow, S.-N. and Hsieh, F.-J.; MING-KWANG SHYU; CHIEN-NAN LEE |
| 國立臺灣大學 |
2002 |
Prenatal Diagnosis and Treatment of Fetal Long Qt Syndrome: A Case Report
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張銀光; 徐明洸; 李建南; 高妙玲; 柯玉雪; 周松男; 謝豐舟; CHANG, ING-KUANG; SHYU, MING-KWANG; LEE, CHIEN-NAN; KAO, MIAO-LING; KO, YU-HSUEH; CHOW, SONG-NAN; HSIEH, FON-JOU |
| 臺大學術典藏 |
2020-02-12T04:06:39Z |
Prenatal diagnosis and treatment of fetal long QT syndrome: A case report
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Hsieh F.-J.;Chow S.-N;Ko Y.-H;Kau M.-L;CHIEN-NAN LEE;Shyu M.-K;Chang I.-K; Chang I.-K; Shyu M.-K; CHIEN-NAN LEE; Kau M.-L; Hsieh F.-J.; Ko Y.-H; Chow S.-N |
| 臺大學術典藏 |
2020-02-14T05:49:48Z |
Prenatal diagnosis and treatment of fetal long QT syndrome: A case report
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MING-KWANG SHYU; Lee C.-N; Kau M.-L; Ko Y.-H; Chow S.-N; Hsieh F.-J.; Chang I.-K;Ming-Kwang Shyu;Lee C.-N;Kau M.-L;Ko Y.-H;Chow S.-N;Hsieh F.-J.; Chang I.-K |
| 臺大學術典藏 |
2021-02-04T06:05:22Z |
Prenatal diagnosis and treatment of fetal long QT syndrome: A case report
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Chang I.-K.;Shyu M.-K.;Chien-Nan Lee;Kau M.-L.;Ko Y.-H.;Chow S.-N.;Hsieh F.-J.; Chang I.-K.; Shyu M.-K.; CHIEN-NAN LEE; Kau M.-L.; Ko Y.-H.; Chow S.-N.; Hsieh F.-J. |
| 臺大學術典藏 |
2018-09-10T05:14:34Z |
Prenatal diagnosis by transabdominal chorionic villus sampling in the second and third trimesters
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Ko, T.-M.;Tseng, L.-H.;Hwa, H.-L.;Lee, T.-Y.;Chuang, S.-M.; LI-HUI TSENG; HSIAO-LIN HWA |
| 臺大學術典藏 |
2020-02-03T08:15:27Z |
Prenatal diagnosis by transabdominal chorionic villus sampling in the second and third trimesters
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Lee T.-Y.; Chuang S.-M.; Ko T.-M.;Tseng L.-H.;Hsiao-Lin Hwa;Lee T.-Y.;Chuang S.-M.; Ko T.-M.; Tseng L.-H.; HSIAO-LIN HWA |
| 臺大學術典藏 |
2022-03-10T07:58:57Z |
Prenatal diagnosis by transabdominal chorionic villus sampling in the second and third trimesters
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Ko T.-M.; LI-HUI TSENG; Hwa H.-L.; Lee T.-Y.; Chuang S.-M. |
| 亞洲大學 |
2016-02 |
Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion
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Chen), Yen-Ni Chen(Yen-Ni;陳持平*;Ko), Tsang-Ming K(Tsang-Ming;Wang), Liang-Kai Wa(Liang-Kai;Wu), Pei-Chen Wu(Pei-Chen;Chang), Tung-Yao Cha(Tung-Yao;Wu), Peih-Shan Wu(Peih-Shan;Yang), Chien-Wen Ya(Chien-Wen;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2016-02 |
Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion
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Chen, Yen-Ni;Chen, Yen-Ni;陳持平*;Tsang-Ming, K;Ko, Tsang-Ming;Wa, Liang-Kai;Wang, Liang-Kai;Wu, Pei-Chen;Wu, Pei-Chen;Cha, Tung-Yao;Chang, Tung-Yao;Wu, Peih-Shan;Wu, Peih-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-02 |
Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion
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Wang；, Yen-Ni Chen；Yen-Ni Chen；陳持平*；Tsang-Ming K；Tsang-Ming Ko；Liang-Kai Wa；Liang-Kai Wang；Pei-Chen Wu；Pei-Chen Wu；Tung-Yao Cha；Tung-Yao Chang；Peih-Shan Wu；Peih-Shan Wu；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen |
| 臺大學術典藏 |
2020-02-14T02:50:41Z |
Prenatal diagnosis of 46, XX/47, XXY mosaicism: A case report
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Cheng W.?F.; Huang S.?C.; Ko T.?M. |
| 亞洲大學 |
2009-03 |
PRENATAL DIAGNOSIS OF 46,XX,DER(13;21)(Q10;Q10),+21 AND TRANSIENT ABNORMAL MYELOPOIESIS IN A FETUS WITH HEPATOSPLENOMEGALY AND SPONTANEOUS RESOLUTION OF FETAL ASCITES
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Chen, CP (Chen, Chih-Ping); Tsai, FJ (Tsai, Fuu-Jen); Chern, SR (Chern, Schu-Rern); Chang, TY (Chang, Tung-Yao); Hsu, CY (Hsu, Chin-Yuan); Lin, HH (Lin, Hung-Hung); Wang, W (Wang, Wayseen) |
| 亞洲大學 |
2009-03 |
PRENATAL DIAGNOSIS OF 46,XX,DER(13;21)(Q10;Q10),+21 AND TRANSIENT ABNORMAL MYELOPOIESIS IN A FETUS WITH HEPATOSPLENOMEGALY AND SPONTANEOUS RESOLUTION OF FETAL ASCITES
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陳持平;Chen, Chih-Ping;Tsai, Fuu-Jen;Chern, Schu-Rern;Chang, Tung-Yao;Hsu, Chin-Yuan;Lin, Hung-Hung;Wang, Wayseen |
| 中國醫藥大學 |
2009-03 |
Prenatal diagnosis of 46,XX,der(13;21)(q10;q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites
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陳持平(Chih-Ping Chen); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Tung-Yao Chang); (Chin-Yuan Hsu); (Hung-Hung Lin); (Wayseen Wang) |
| 亞洲大學 |
2018-02 |
Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities
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陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;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;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2017-12 |
Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones
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陳持平;Chen, Chih-Ping;Chen, Chen-Yu;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;Chen, Li-Feng;Wang, Wayseen |
| 亞洲大學 |
2009-12 |
Prenatal diagnosis of a 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect by array comparative genomic hybridization
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chang, Tung-Yao;Chern, Schu-Rern;Tsai, Fuu-Jen;Hwang, Jonathan Kwei;Wang, Wayseen |
| 亞洲大學 |
2018-08 |
Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability
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陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Chen, Wen-Lin;Chen, Wen-Lin;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 國立臺灣大學 |
2010 |
Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 -> Q11.23 by Array Comparative Genomic Hybridization
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陳持平; 蘇怡寧; 陳樹人; 蔡輔仁; 徐金源; 李貞姫; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; HSU, CHIN-YUAN; LEE, CHEN-CHI; WANG, WAYSEEN |
| 中國醫藥大學 |
2010-03 |
Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization
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陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Chen-Chi Lee); (Wayseen Wang) |
Showing items 682826-682850 of 2349128 (93966 Page(s) Totally)
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View [10|25|50] records per page
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