| 中國醫藥大學 |
2012-09 |
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Schu-Rern Chern);(Jun-Wei Su);(Yu-Ting Chen);(Chen-Chi Lee);(Wayseen Wang) |
| 亞洲大學 |
2015-10 |
Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome and Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1
|
Wang, 陳持平；Ming-Huei Li；Ming-Huei Lin；Yi-Yung Chen；Yi-Yung Chen；Schu-Rern Ch；Schu-Rern Chern；Yen-Ni Chen；Yen-Ni Chen；Peih-Shan Wu；Peih-Shan Wu；Chen-Wen Pan；Chen-Wen Pan；Meng-Shan Le；Meng-Shan Lee；Wayseen Wang；Wayseen |
| 亞洲大學 |
2015-10 |
Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome and Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1
|
陳持平*;Lin), Ming-Huei Li(Ming-Huei;Chen), Yi-Yung Chen(Yi-Yung;Chern), Schu-Rern Ch(Schu-Rern;Chen), Yen-Ni Chen(Yen-Ni;Wu), Peih-Shan Wu(Peih-Shan;Pan), Chen-Wen Pan(Chen-Wen;Lee), Meng-Shan Le(Meng-Shan;Wang), Wayseen Wang(Wayseen |
| 中國醫藥大學 |
2015-10 |
Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome and Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1
|
陳持平(Chih-Ping Chen)*;(Ming-Huei Lin);(Yi-Yung Chen);(Schu-Rern Chern);(Yen-Ni Chen);(Peih-Shan Wu);(Chen-Wen Pan);(Meng-Shan Lee);(Wayseen Wang) |
| 亞洲大學 |
2015-02 |
Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap
|
陳持平*;Wan, Yeou-Lih;Wang, Yeou-Lih;Ch, Schu-Rern;Chern, Schu-Rern;Liu, Yu-Peng;Liu, Yu-Peng;Pe, Cheng-Ran;Peng, Cheng-Ran;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201502 |
Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap
|
Wan, 陳持平*; Yeou-Lih;Wang, Yeou-Lih;Ch, Schu-Rern;Chern, Schu-Rern;Liu, Yu-Peng;Liu, Yu-Peng;Pe, Cheng-Ran;Peng, Cheng-Ran;Kuo, Yu-Ling;Kuo, Yu-Ling;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap
|
Wang, 陳持平；Yeou-Lih Wan；Yeou-Lih Wang；Schu-Rern Ch；Schu-Rern Chern；Yu-Peng Liu；Yu-Peng Liu；Cheng-Ran Pe；Cheng-Ran Peng；Yu-Ling Kuo；Yu-Ling Kuo；Peih-Shan Wu；Peih-Shan Wu；Wen-Lin Chen；Wen-Lin Chen；Wayseen Wang；Wayseen |
| 中國醫藥大學 |
2015-02 |
Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap
|
陳持平(Chih-Ping Chen)*;(Yeou-Lih Wang);(Schu-Rern Chern);(Yu-Peng Liu);(Cheng-Ran Peng);(Yu-Ling Kuo);(Peih-Shan Wu);(Wen-Lin Chen);(Wayseen Wang) |
| 臺大學術典藏 |
2018-09-10T04:43:53Z |
Prenatal diagnosis and corticosteroid treatment of diffuse neonatal hemangiomatosis: Case report
|
Sheu, B.-C. and Shyu, M.-K. and Lin, Y.-F. and Lee, C.-N. and Hsieh, F.-J. and Chou, Y.-H. and Yau -, K.I.T. and Huang, S.-F.; MING-KWANG SHYU |
| 臺大學術典藏 |
2018-09-10T05:03:17Z |
Prenatal diagnosis and corticosteroid treatment of diffuse neonatal hemangiomatosis: Case report
|
Sheu, B.-C. and Shyu, M.-K. and Lin, Y.-F. and Lee, C.-N. and Hsieh, F.-J. and Chou, Y.-H. and Yau -, K.I.T. and Huang, S.-F.; CHIEN-NAN LEE; BOR-CHING SHEU |
| 臺大學術典藏 |
2020-01-22T06:00:44Z |
Prenatal diagnosis and corticosteroid treatment of diffuse neonatal hemangiomatosis: Case report
|
BOR-CHING SHEU; Shyu M.-K.; Lin Y.-F.; Lee C.-N.; Hsieh F.-J.; Chou Y.-H.; Yau - K.I.T.; Huang S.-F. |
| 臺大學術典藏 |
2020-02-12T04:07:05Z |
Prenatal diagnosis and corticosteroid treatment of diffuse neonatal hemangiomatosis: Case report
|
Huang S.-F.;Yau - K.I.T;Chou Y.-H;Hsieh F.-J;CHIEN-NAN LEE;Lin Y.-F;Shyu M.-K;Sheu B.-C; Sheu B.-C; Shyu M.-K; Lin Y.-F; CHIEN-NAN LEE; Hsieh F.-J; Chou Y.-H; Yau - K.I.T; Huang S.-F. |
| 臺大學術典藏 |
2020-02-14T05:49:56Z |
Prenatal diagnosis and corticosteroid treatment of diffuse neonatal hemangiomatosis: Case report
|
Sheu B.-C; MING-KWANG SHYU; Lin Y.-F; Lee C.-N; Hsieh F.-J; Chou Y.-H; Yau - K.I.T; Huang S.-F. |
| 國立臺灣大學 |
1994 |
Prenatal Diagnosis and Corticosteroid Treatment of Diffuse Neonatal Hemangiomatosis:Case Report
|
Sheu, Bor-Ching; Shyu, Ming-Kwang; Lin, Yu-Feng; Lee, Chien-Nan; 謝豐舟; Chou, Yi-Hong; 鄒國英; Sheu, Bor-Ching; Shyu, Ming-Kwang; Lin, Yu-Feng; Lee, Chien-Nan; Hsieh, Fon-Jou; Chou, Yi-Hong; Yau Tsou, Kuo-Inn |
| 臺大學術典藏 |
2018-09-10T05:45:11Z |
Prenatal diagnosis and genetic analysis of a fetus with 47, XX,+21/46,XX mosaicism and XX/XY chimerism
|
Hwa, H.-L. and Ko, T.-M. and Huang, C.-H. and Chang, L.-S.; HSIAO-LIN HWA |
| 臺大學術典藏 |
2020-02-03T08:15:22Z |
Prenatal diagnosis and genetic analysis of a fetus with 47, XX,+21/46,XX mosaicism and XX/XY chimerism
|
HSIAO-LIN HWA; Ko T.-M.; Huang C.-H.; Chang L.-S. |
| 國立臺灣大學 |
2006 |
Prenatal Diagnosis and Genetic Analysis of a Fetus with 47,Xx,+21/46,Xx Mosaicism and Xx/Xy Chimerism
|
華筱玲; 柯滄銘; 張麗束; HWA, HSIAO-LIN; KO, TSANG-MING; CHANG, LI-SHU |
| 亞洲大學 |
2012-03 |
Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review
|
陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2012-03 |
Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review
|
陳持平(Chih-Ping Chen)* |
| 國立臺灣大學 |
2001 |
Prenatal Diagnosis and Genetic Analysis of Type I and Type Ii Thanatophoric Dysplasia
|
陳持平; 陳樹人; 施景中; 王偉信; 張東耀; 曾岐元; CHEN, CHIH-PING; CHERN, SCHU-RERN; SHIH, JIN-CHUNG; WANG, WAYSEEN; CHANG, TUNG-YAO; TZEN, CHIN-YUAN |
| 臺大學術典藏 |
2021-02-04T06:46:59Z |
Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia
|
Chen C.-P.;Chern S.-R.;Jin-Chung Shih;Wang W.;Yeh L.-F.;Chang T.-Y.;Tzen C.-Y.; Chen C.-P.; Chern S.-R.; JIN-CHUNG SHIH; Wang W.; Yeh L.-F.; Chang T.-Y.; Tzen C.-Y. |
| 中國醫藥大學 |
2010-03 |
PRENATAL DIAGNOSIS AND GENETIC COUNSELING FOR MOSAIC TRISOMY 13
|
陳持平(Chih-Ping Chen)* |
| 亞洲大學 |
2010-03 |
Prenatal diagnosis and genetic counseling of mosaic trisomy 13
|
陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2007-03 |
Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome)
|
陳持平(Chih-Ping Chen)*; 林炫沛(Shuan-Pei Lin); 曾嶔元(Chin-Yuan Tzen); 胡務亮(Wuh-Liang Hwu); 陳樹人(Schu-Rern Chern); 莊志光(Chih-Kuang Chuang); 蔣淑清(Shu-Shien Chien); 王偉信(Wayseen Wang) |
| 臺大學術典藏 |
2020-12-16T02:26:01Z |
Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome)
|
Chen C.-P.;Lin S.-P.;Tzen C.-Y.;Wuh-Liang Hwu;Chern S.-R.;Chuang C.-K.;Chiang S.-S.;Wang W.; Chen C.-P.; Lin S.-P.; Tzen C.-Y.; WUH-LIANG HWU; Chern S.-R.; Chuang C.-K.; Chiang S.-S.; Wang W. |
