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Showing items 682821-682870 of 2349128 (46983 Page(s) Totally)
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| 中國醫藥大學 |
2012-06 |
Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene
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陳持平(Chih-Ping Chen)*;(Schu-Rern Chern);(Tung-Yao Chang);(Yi-Ning Su);(Yi-Yung Chen);(Jun-Wei Su);(Wayseen Wang) |
| 臺大學術典藏 |
2018-09-10T06:48:26Z |
Prenatal diagnosis and perinatal outcome of facial clefts
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Pan, Y.-J. and Shih, J.-C. and Lee, C.-N. and Shyu, M.-K. and Hwa, H.-L. and Chen, H.-Y. and Hsieh F.-, J.; HSIAO-LIN HWA |
| 臺大學術典藏 |
2018-09-10T06:50:05Z |
Prenatal diagnosis and perinatal outcome of facial clefts
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Pan, Y.-J. and Shih, J.-C. and Lee, C.-N. and Shyu, M.-K. and Hwa, H.-L. and Chen, H.-Y. and Hsieh F.-, J.; MING-KWANG SHYU |
| 臺大學術典藏 |
2018-09-10T07:14:01Z |
Prenatal diagnosis and perinatal outcome of facial clefts
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Pan, Y.-J. and Shih, J.-C. and Lee, C.-N. and Shyu, M.-K. and Hwa, H.-L. and Chen, H.-Y. and Hsieh F.-, J.; CHIEN-NAN LEE |
| 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. |
| 臺大學術典藏 |
2020-02-14T05:49:52Z |
Prenatal diagnosis and perinatal outcome of facial clefts
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Pan Y.-J; Shih J.-C; Lee C.-N; MING-KWANG SHYU; 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
|
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
|
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
|
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
|
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
|
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 |
| 亞洲大學 |
2010-03 |
Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization
|
陳持平;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
|
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) |
| 亞洲大學 |
2011-12 |
Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly
|
陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2014-12 |
Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies
|
(Wen-Chien Hou);陳持平(Chih-Ping Chen);(Kwei-Shuai Hwang);(Ying-Chieh Chen);(Yu-Ju Lai);(Chau-Yang Tien);(Her-Young Su)* |
| 亞洲大學 |
2011-12 |
Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction
|
陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2011-12 |
Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction
|
(Yi-Hui Lin);陳持平(Chih-Ping Chen)*;(Tze-Chien Chen);(Chun-Sen Hsu);(Szu-Yuan Chou);簡淑錦(Shu-Chin Chien) |
| 亞洲大學 |
2018-10 |
Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound
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陳持平;Chen, Chih-Ping;Cha, Shu-Yuan;Chang, Shu-Yuan;Wa, Liang-Kai;Wang, Liang-Kai;Cha, Tung-Yao;Chang, Tung-Yao;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, hin-Wen;Chen, hin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen |
| 亞洲大學 |
2018-10 |
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound
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陳持平;Chen, Chih-Ping;Cha, Shu-Yuan;Chang, Shu-Yuan;Chen, Yen-Ni;Chen, Yen-Ni;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;Chen, Li-Feng;Chen, Li-Feng |
| 亞洲大學 |
2018-10 |
Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound
|
陳持平;Chen, Chih-Ping;Cha, Shu-Yuan;Chang, Shu-Yuan;Lin, Chen-Ju;Lin, Chen-Ju;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;Lai, hih-Ting;Lai, hih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Chen, Wen-Lin;Chen, Wen-Lin;Ya, Chien-Wen;Yang, Chien-Wen |
| 國立臺灣大學 |
2004 |
Prenatal Diagnosis of a Fetus Affected with down Syndrome and Deletion 1p 36 Syndrome by Fluorescence in Situ Hybridization and Spectral Karyotyping
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謝聰哲; 葉光芃; 陳明; 王寶田; HSIEH, TSUNG-CHE; YEH, GUANG-PERNG; CHEN, MING; WANG, BAO-TYAN |
| 臺大學術典藏 |
2018-09-10T05:03:07Z |
Prenatal diagnosis of a fetus affected with down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping
|
Hsieh, L.-J.;Hsieh, T.-C.;Yeh, G.-P.;Lin, M.-I.;Chen, M.;Wang, B.B.-T.; MING CHEN |
| 國立臺灣大學 |
2012 |
Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)
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Hung, Chia-Cheng; Lin, Chia-Hui; Lin, Shin-Yu; Shin, Jin-Chung; Lee, Chien-Nan; Su, Yi-Ning; 林芯?; 蘇怡寧; 李建南; 林佳慧 |
| 臺大學術典藏 |
2018-09-10T09:27:32Z |
Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)
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Lee, Chien-Nan; Su, Yi-Ning; Shin, Jin-Chung; Lin, Chia-Hui; Lin, Shin-Yu; CHIEN-NAN LEE; SHIN-YU LIN; Hung, Chia-Cheng; 林芯?;蘇怡寧;李建南;林佳慧; Hung, Chia-Cheng;Lin, Chia-Hui;Lin, Shin-Yu;Shin, Jin-Chung;Lee, Chien-Nan;Su, Yi-Ning; Hung, C.-C. and Lin, C.-H. and Lin, S.-Y. and Shin, J.-C. and Lee, C.-N. and Su, Y.-N. |
| 臺大學術典藏 |
2020-02-12T04:05:56Z |
Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)
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Su Y.-N.;CHIEN-NAN LEE;Shin J.-C;Lin S.-Y;Lin C.-H;Hung C.-C; Hung C.-C; Lin C.-H; Lin S.-Y; Shin J.-C; CHIEN-NAN LEE; Su Y.-N. |
| 臺大學術典藏 |
2021-02-04T06:47:07Z |
Prenatal diagnosis of a fetus with distal 10q trisomy
|
Chen C.-P.;Jin-Chung Shih;Lee C.-C.;Chen L.-F.;Wang W.;Wang T.-Y.; Chen C.-P.; JIN-CHUNG SHIH; Lee C.-C.; Chen L.-F.; Wang W.; Wang T.-Y. |
| 國立成功大學 |
2001-06 |
Prenatal diagnosis of a fetus with megacystis and monosomy 21
|
Chang, Ling-Wei; Chen, Pei-Yi; Kuo, Pao-Lin; Chang, Fong-Ming |
| 中國醫藥大學 |
2006 |
Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32->qter)and partial monosomy 21q(21q22.2->qter).
|
陳持平(Chen CP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,) |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome
|
陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Su, Yi-Ning;Su, Yi-Ning;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome
|
陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);(Schu-Rern Chern);(Jun-Wei Su);(Wayseen Wang) |
| 國立臺灣大學 |
1993 |
Prenatal Diagnosis of a Succenturiate Placenta:A Case Report
|
Chang, Chung-Ching; Su, Chu'ng-Guei; 柯滄銘; Chang, Chung-Ching; Su, Chu'ng-Guei; Ko, Tsang-Ming |
| 國立成功大學 |
2003-02 |
Prenatal diagnosis of a triplet pregnancy complicated with one acardius in a patient with didelphys uterus using three-dimensional ultrasound
|
Chang, Ling-Wei; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Chang, Fong-Ming |
Showing items 682821-682870 of 2349128 (46983 Page(s) Totally)
<< < 13652 13653 13654 13655 13656 13657 13658 13659 13660 13661 > >>
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