| 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) |
| 中國醫藥大學 |
2009-09 |
Prenatal diagnosis of and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly
|
陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Kevin Ko); (Wayseen Wang) |
| 中國醫藥大學 |
2009-09 |
Prenatal diagnosis of and molecular analysis of trisomy 13 mosaicism
|
陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Chen-Wen Pan); (Wayseen Wang) |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3->q23.3) associated with abnormal maternal serum biochemistry
|
陳持平;Chen, Chih-Ping;Su, Yi-Ning;Su, Yi-Ning;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis of and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3->q23.3) associated with abnormal maternal serum biochemistry
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Shuan-Pei Lin);(Schu-Rern Chern);(Jun-Wei Su);(Yu-Ting Chen);(Meng-Shan Lee);(Wayseen Wang) |
| 中國醫藥大學 |
1998 |
Prenatal diagnosis of Apert syndrome
|
Chang, CC; Tsai, FJ; Tsai, HD; Tsai, CH; Hsieh, YY; Lee, CC; Yang, TC; Wu, JY |
| 中國醫藥大學 |
2007-06 |
Prenatal diagnosis of atypical facial clefting should alert amniotic band syndrome and prompt a search for associated amniotic bands and other structural anomalies
|
陳持平(Chih-Ping Chen)* |
| 臺大學術典藏 |
2021-02-04T06:47:06Z |
Prenatal diagnosis of bilateral ventriculomegaly and an enlarged cisterna magna in a fetus with partial trisomy 9 and partial trisomy 21 [1]
|
Chen C.-P.;Jin-Chung Shih; Chen C.-P.; JIN-CHUNG SHIH |
| 國立臺灣大學 |
2003 |
Prenatal Diagnosis of Cephalothoracopagus Janiceps Disymmetros Using Three-Dimensional Power Doppler Ultrasound and Magnetic Resonance Imaging
|
施景中; SHIH, JIN-CHUNG |
| 臺大學術典藏 |
2018-09-10T04:32:16Z |
Prenatal diagnosis of cephalothoracopagus janiceps disymmetros using three-dimensional power Doppler ultrasound and magnetic resonance imaging
|
Chen, C.-P. and Shih, J.-C. and Shih, S.-L. and Huang, J.-K. and Huang, J.-P. and Lin, Y.-H. and Wang, W.; JIN-CHUNG SHIH |
| 臺大學術典藏 |
2021-02-04T06:46:55Z |
Prenatal diagnosis of cephalothoracopagus janiceps disymmetros using three-dimensional power Doppler ultrasound and magnetic resonance imaging
|
Chen C.-P.;Jin-Chung Shih;Shih S.-L.;Huang J.-K.;Huang J.-P.;Lin Y.-H.;Wang W.; Chen C.-P.; JIN-CHUNG SHIH; Shih S.-L.; Huang J.-K.; Huang J.-P.; Lin Y.-H.; Wang W. |
| 亞洲大學 |
2011-06 |
Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene
|
陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2011-06 |
Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Chin-Yuan Hsu);(Ming-Ren Chen);(Yu-Peng Liu);(Pei-Chen Wu);(Wayseen Wang) |
| 國立臺灣大學 |
1990 |
Prenatal Diagnosis of Chinese Homozygous Alpha-Thalassemia 1 and Haemoglobin H Disease by Analysis of Alpha-and Pseudo-Zeta-Globin Genes in Chorionic Villi and Amniocytes
|
柯滄銘; 謝豐舟; Lee, Tzu-Yao; Ko, Tsang-Ming; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 國立臺灣大學 |
1989 |
Prenatal Diagnosis of Chinese Homozyous a-Thalassaemia 1 and Haemoglobin H Disease by Anbalysis of a-and-Globin Genes in Chorionic Villi and Amniocytes
|
Ko, T. M.; 謝豐舟; 李鎡堯; Ko, T. M.; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 中國醫藥大學 |
2015-12 |
Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly
|
陳持平(Chih-Ping Chen)*;(Cheng-Ran Peng);(Tung-Yao Chang);(Wan-Yuo Guo);(Yen-Ni Chen);(Peih-Shan Wu);(Dai-Dyi Town);(Wayseen Wang) |
| 國立臺灣大學 |
1990 |
Prenatal Diagnosis of Chromosome Mosaic 46, XY/46, XY, i(17q) by Amniocentesis:Report of One Case
|
Perng, Bao-Chin; 柯滄銘; 謝豐舟; Lee, Tzu-Yao; Perng, Bao-Chin; Ko, Tsang-Ming; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 國立臺灣大學 |
1990 |
PRENATAL DIAGNOSIS OF CHROMOSOME MOSAIC 46,XY/46,XY,i(17q)BY AMNIOCENTESIS - REPORT OF ONE CASE
|
柯滄銘; 謝豐舟; 李鎡堯; PERNG, BAO-CHIN; KO, TSANG-MING; HSIEH, FON-JOU; LEE, TZU-YAO |
| 國立成功大學 |
2001-08 |
Prenatal diagnosis of cleft palate by three-dimensional ultrasound
|
Chen, Min-Long; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Cheng, Yueh-Chin; Chang, Fong-Ming |
| 中國醫藥大學 |
2014-06-21 |
Prenatal diagnosis of coarctation of the aorta
|
裘品筠;彭義欽;莊子瑤;張正成(Jeng-Sheng Chang);裘品筠;張正成(Jeng-Sheng Chang) |
| 臺大學術典藏 |
2020-03-04T08:52:28Z |
Prenatal diagnosis of coarctation of the aorta with ventricular septal defect: A case report
|
Huang Y.-L.;Hsu K.-H.;Chuluunbaatar E.;Wen T.-M.;Li Y.-Y.;Chen M.-R.;Chung-I Chang;Chang T.-Y.; Huang Y.-L.; Hsu K.-H.; Chuluunbaatar E.; Wen T.-M.; Li Y.-Y.; Chen M.-R.; CHUNG-I CHANG; Chang T.-Y. |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes
|
Chen, CP; Chen, CY; Lin, CY; Shaw, SW; Wang, WS; Tzen, CY |
| 亞洲大學 |
2020-01-20 |
Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects
|
Ch, Chih-Ping;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Che, Shin-Wen;Chen, Shin-Wen;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Wu, Fang-Tzu;Wu, Fang-Tzu;Chen, Wen-Lin;Chen, Wen-Lin;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen |
| 中國醫藥大學 |
2007.05 |
Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution.
|
陳持平(Chen CP)*; 劉玉鵬(Liu YP); 簡淑錦(Shu-Chin Chien); 王偉信(Wang W) |
| 中國醫藥大學 |
2008-05 |
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand foot malformation associated with partial monosomy 4p (4p16.1->pter) and partial trisomy 10q (10q25.1->qter)
|
陳持平(Chih-Ping Chen); (Yann-Jang Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Tung-Yao Chang); (Chen-Chi Lee); (Dai-Dyi Town); (Meng-Shan Lee); (Wayseen Wang) |
| 亞洲大學 |
2008-05 |
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1 -> pter) and partial trisomy 10q (10q25.1 -> qter)
|
Chen, CP (Chen, Chih-Ping); Chen, YJ (Chen, Yann-Jang); Chern, SR (Chern, Schu-Rern); Tsai, FJ (Tsai, Fuu-Jen); Chang, TY (Chang, Tung-Yao); Lee, CC (Lee, Chen-Chi); Town, DD (Town, Dai-Dyi); Lee, MS (Lee, Meng-Shan); Wang, W (Wang, Wayseen) |
