| 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 |
| 國立臺灣大學 |
2007 |
Prenatal Diagnosis and Genetic Counseling of Mucopolysaccharidosis Type Ii (Hunter Syndrome)
|
陳持平; 林炫沛; 曾岐元; 胡務亮; 陳樹人; 王偉信; CHEN, CHIH-PING; LIN, SHUAN-PEI; TZEN, CHIN-YUAN; HWU, WUH-LIANG; CHERN, SCHU-RERN; WANG, WAY-SEEN |
| 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. |
| 亞洲大學 |
2009-02 |
PRENATAL DIAGNOSIS and GENETIC COUNSELING of NEURAL TUBE DEFECTS-An OVERVIEW and ATLAS of CASES
|
陳持平;Chen, Chih-Ping |
| 國立臺灣大學 |
1989 |
Prenatal Diagnosis and Management of Surgically Correctable Fetal Malformations
|
謝豐舟; Lin, C. R.; 陳維昭; Chen, C. C.; Tsai. T. C.; Hsieh, Fon-Jou; Lin, C. R.; Chen, Wei-Jao; Chen, C. C.; Tsai. T. C. |
| 亞洲大學 |
2009-09 |
PRENATAL DIAGNOSIS AND MOLECULAR ANALYSIS OF TRIPLOIDY IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, RELATIVE MACROCEPHALY AND HOLOPROSENCEPHALY
|
Chih-Ping Chen;Schu-Rern Chern;Fuu-Jen Tsai;Chin-Yuan Hsu;Kevin Ko;Wayseen Wang |
| 亞洲大學 |
2009-09 |
Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly
|
陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Ko, Kevin;Wang, Wayseen |
| 亞洲大學 |
2009-09 |
PRENATAL DIAGNOSIS AND MOLECULAR ANALYSIS OF TRISOMY 13 MOSAICISM
|
Chih-Ping Chen;Schu-Rern Chern;Fuu-Jen Tsai;Hung-Hung Lin;Chen-Wen Pan;Wayseen Wang |
| 亞洲大學 |
2009-09 |
Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism
|
陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Lin, Hung-Hung;Pan, Chen-Wen;Wang, Wayseen |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3 -> qter) and partial trisomy 18q (18q23 -> qter) in a fetus associated with cystic hygroma and ambiguous genitalia
|
Chen, CP; Chern, SR; Wang, TH; Hsueh, DW; Lee, CC; Town, DD; Wang, WS; Ko, TM |
