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顯示項目 682831-682880 / 2349128 (共46983頁)
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機構	日期	題名	作者
臺大學術典藏	2018-09-10T04:05:34Z	Prenatal diagnosis and treatment of fetal long QT syndrome: A case report	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	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	2020-02-14T05:49:48Z	Prenatal diagnosis and treatment of fetal long QT syndrome: A case report	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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)	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)	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)	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
中國醫藥大學	2002	Prenatal diagnosis of abdominal lymphangioma	Ho, M; Lee, CC; Lin, TY
中國醫藥大學	2002-08	Prenatal diagnosis of abdominal lymphangioma	何銘(Ming- Ho); 李建忠(C.C Lee); 林智一(Tze-Yi Lin)
國立成功大學	2000-05	Prenatal diagnosis of alobar holoprosencephaly by two-dimensional and three-dimensional ultrasound	Lai, Tsung-Hsuan; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Kuo, Pao-Lin; Chang, Fong-Ming
亞洲大學	2017-12	Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound	陳持平;Chen, Chih-Ping;Cha, Tung-Yao;Chang, Tung-Yao;Hung, Fang-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;Lee, Chen-Chi;Wang, Wayseen
國立臺灣大學	2005	Prenatal Diagnosis of an Acardiac Amorphous Twin and the Anomalous Co- Twin in a Monoamniotic Twin Pregnancy	陳持平; 施景中; 陳樹人; 林靜宜; 王偉信; 曾岐元; CHEN, CHIH-PING; SHIH, JIN-CHUNG; CHERN, SCHU-RERN; LIN, CHING-YI; WANG, WAYSEEN; TZEN, CHIN-YUAN
國立臺灣大學	2005-06	PRENATAL DIAGNOSIS OF AN ACARDIAC AMORPHOUS TWIN AND THE ANOMALOUS CO-TWIN IN A MONOAMNIOTIC TWIN PREGNANCY	陳持平; 施景中; 陳樹人; 林靜宜; 王偉信; 曾岐元
中國醫藥大學	2005	Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy	Chen, CP; Shih, JC; Chang, TY; Chern, SR; Lin, CY; Wang, WS; Tzen, CY
臺大學術典藏	2021-02-04T06:46:51Z	Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy [4]	Chen C.-P.;Jin-Chung Shih;Chang T.-Y.;Chern S.-R.;Lin C.-Y.;Wang W.;Tzen C.-Y.; Chen C.-P.; JIN-CHUNG SHIH; Chang T.-Y.; Chern S.-R.; Lin C.-Y.; Wang W.; Tzen C.-Y.
中國醫藥大學	2012-12	Prenatal diagnosis of an interstitial deletion of 10q (10q11.21->q21.1): array comparative genomic hybridization characterization and literature review	陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Dai-Dyi Town);(Wayseen Wang)
中國醫藥大學	2008-03-15	prenatal diagnosis of an XX male with the SRY gene on chromosome 3p	簡淑錦(Shu-Chin Chien)

顯示項目 682831-682880 / 2349128 (共46983頁)
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