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Institution	Date	Title	Author
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
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
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
中國醫藥大學	2014-12	Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome	陳持平(Chih-Ping Chen)*;(Chen-Ju Lin);(Schu-Rern Chern);(Yu-Peng Liu);(Yu-Ling Kuo);(Peih-Shan Wu);(Dai-Dyi Town);(Li-Feng Chen);(Chien-Wen Yang);(Wayseen Wang)
亞洲大學	2016-04	Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot	Chen)*, 陳持平(Chih-Ping;Chen), Chen-Yu Chen(Chen-Yu;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(Shin-Wen;Chen), Li-Feng Chen(Li-Feng;Yang), Chien-Wen Ya(Chien-Wen;Wang), Wayseen Wang(Wayseen
亞洲大學	2016-04	Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot	陳持平;Chen, Chih-Ping;*;Chen, Chen-Yu;Chen, Chen-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學	2016-04	Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot	Wang；, 陳持平；Chih-Ping Chen；*；Chen-Yu Chen；Chen-Yu Chen；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Li-Feng Chen；Li-Feng Chen；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen
亞洲大學	2013-06	Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1->q31.1)	陳持平;Chen, Chih-Ping;Shing-Jyh Chang;Schu-Rern Chern;Peih-Shan Wu;Yu-Ting Chen;Jun-Wei Su;Wen-Lin Chen;Wayseen Wang
中國醫藥大學	2013-06	Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1->q31.1)	陳持平(Chih-Ping Chen)*;(Shing-Jyh Chang,);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Jun-Wei Su);(Wen-Lin Chen);(Wayseen Wang)
亞洲大學	2013	Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3->q32.12) associated with abnormal maternal serum biochemistry	陳持平;Chen, Chih-Ping;Kwui-Shuai Hwang;Her-Young Su;Shuan-Pei Lin;Yi-Ning Suk, Schu-Rern Chern;Jun-Wei Su;Yu-Ting Chen;Wen-Lin Chen;Wayseen Wang
中國醫藥大學	2013-03	Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3->q32.12) associated with abnormal maternal serum biochemistry	陳持平(Chih-Ping Chen)*;(Kwui-Shuai Hwang);(Her-Young Su);(Shuan-Pei Lin);(Yi-Ning Su);(Schu-Rern Chern);(Yu-Ting Chen);(Jun-Wei Su);(Wen-Lin Chen);(Wayseen Wang)
亞洲大學	2013-10	Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2->p14)	陳持平;Chen, Chih-Ping;Meng-Ju Lee;Schu-Rern Chern;Peih-Shan Wu;Jun-Wei Su;Yu-Ting Chen;Meng-Shan Lee;Wayseen Wang
亞洲大學	2013-10	Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2->p14)	陳持平;Chen, Chih-Ping;Meng-Ju Lee;Schu-Rern Chern;Peih-Shan Wu;Jun-Wei Su;Yu-Ting Chen;Meng-Shan Lee;Wayseen Wang
中國醫藥大學	2013-12	Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review	陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Chen-Yu Chen);(Schu-Rern Chern);(Peih-Shan Wu);蘇俊維(Jun-Wei Su);(Chen-Chi Lee);(Li-Feng Chen);(Wayseen Wang)
亞洲大學	2016-08	Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication	Wang；, 陳持平；Chih-Ping Chen；*；Chen-Ju Lin；Chen-Ju Lin；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Chen-Chi Lee；Chen-Chi Lee；Li-Feng Chen；Li-Feng Chen；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen
亞洲大學	2016-08	Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication	陳持平;Chen, Chih-Ping;*;Lin, Chen-Ju;Lin, Chen-Ju;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學	2011-06	Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly	陳持平;Chen, Chih-Ping
臺大學術典藏	2022-03-14T23:45:39Z	Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22	Chen, Chih Ping; MING CHEN; Ma, Gwo Chin; Chang, Shun Ping; Chern, Schu Rern; Chen, Shin Wen; Wu, Fang Tzu; Chen, Wen Lin; Lee, Meng Shan; Chen, Yun Yi; Wang, Wayseen
亞洲大學	2011-09	Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation	陳持平;Chen, Chih-Ping
中國醫藥大學	2011-09	Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation	陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Ming Chen);(Jain-Pei Huang);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Wen-Lin Chen);(Wayseen Wang)
臺大學術典藏	2018-09-10T08:50:12Z	Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation	Chen, C.-P.;Su, Y.-N.;Chen, M.;Huang, J.-P.;Tsai, F.-J.;Wu, P.-C.;Chen, W.-L.;Wang, W.; MING CHEN
亞洲大學	2013-03	Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2->q11.21)	陳持平;Chen, Chih-Ping;Tsang-Ming Ko;Yi-Ning Su;Jun-Wei Su;Yu-Ting Chen;Chen-Chi Lee;Li-Feng Chen;Wayseen Wang
中國醫藥大學	2013-03	Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2->q11.21)	陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Yi-Ning Su);(Jun-Wei Su);(Yu-Ting Chen);(Chen-Chi Lee);(Li-Feng Chen);(Wayseen Wang)

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