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
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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) |
中國醫藥大學 |
2015-10 |
Interphase fluorescence in situ hybridization assisting in prenatal counseling for amniocentesis karyotyping-detected fetal mosaicism
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(Sheng-Yuan Su);(Ho-Yen Chueh);(Ching-Pei Li);(Yao-Lung Chang);(Shuenn-Dyh Chang)*;陳持平(Chih-Ping Chen) |
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
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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) |
中國醫藥大學 |
2015-08 |
Mosaic trisomy 15 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review
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陳持平(Chih-Ping Chen)*;(Schu-Rern Chern);(Yen-Ni Chen);(Peih-Shan Wu);(Chien-Wen Yang);(Li-Feng Chen);(Wayseen Wang) |
中國醫藥大學 |
2015-06 |
Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature
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陳持平(Chih-Ping Chen)*;(Ming-Chao Huang);(Schu-Rern Chern);(Yu-Ling Kuo);(Yen-Ni Chen);(Peih-Shan Wu);(Li-Feng Chen);(Chen-Wen Pan);(Wayseen Wang) |
中國醫藥大學 |
2015-04 |
First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism
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陳持平(Chih-Ping Chen)*;(Liang-Kai Wang);(Schu-Rern Chern);(Yu-Ling Kuo);(Yen-Ni Chen);(Chen-Wen Pan);(Wayseen Wang) |
中國醫藥大學 |
2015-02 |
Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis
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陳持平(Chih-Ping Chen)*;蘇俊維(Jun-Wei Su);(Schu-Rern Chern);(Yu-Ling Kuo);(Peih-Shan Wu);(Meng-Shan Lee);(Chien-Wen Yang);(Wayseen Wang) |
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
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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) |
中國醫藥大學 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma
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陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Ming-Chao Huang);(Schu-Rern Chern);(Tan-Wei Lin);(Tung-Yao Chang);(Yu-Ling Kuo);(Wen-Lin Chen);(Wayseen Wang) |
亞洲大學 |
201403 |
Phenethyl isothiocyanate triggers apoptosis in human malignant melanoma A375.S78 cells through reactive oxygen species and the mitochondria-dependent pathways
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Chen-Ju Lin(Chen-Ju Lin)*; 陳持平(Chih-Ping Chen); Shu-Chin Chi(Shu-Chin Chien); Chen-Chi Lee(Chen-Chi Lee, ); Dai-Dyi Town(Dai-Dyi Town); Wen-Lin Chen(Wen-Lin Chen); L i-Feng Che(L i-Feng Chen); Meng-Shan Le(Meng-Shan Lee); ,(Chen-Wen Pan,); ,(Ku-Chien Lin,); Tze-Tien Yeh(Tze-Tien Yeh); ; ; |
中國醫藥大學 |
2014-12 |
Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome
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陳持平(Chih-Ping Chen)*;(Cheng-Ran Peng);(Schu-Rern Chern);(Yu-Ling Kuo);(Peih-Shan Wu);(Dai-Dyi Town);(Chen-Wen Pan);(Chien-Wen Yang);(Wayseen Wang) |
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
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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) |
中國醫藥大學 |
2014-12 |
First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination
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陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Chen-Yu Chen);(Tao-Yeuan Wang);(Schu-Rern Chern);(Yu-Ling Kuo);(Wayseen Wang) |
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
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(Wen-Chien Hou);陳持平(Chih-Ping Chen);(Kwei-Shuai Hwang);(Ying-Chieh Chen);(Yu-Ju Lai);(Chau-Yang Tien);(Her-Young Su)* |
中國醫藥大學 |
2014-06 |
Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects
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Yu-Ling Kuo;陳持平(Chih-Ping Chen)*;(Liang-Kai Wang);(Tsang-Ming Ko);(Tung-Yao Chang);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Shu-Yuan Chang) |
亞洲大學 |
2014-03 |
Chromosomal deletions detected at amniocentesis
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Chen-Ju Lin(Chen-Ju Lin)*; 陳持平(Chih-Ping Chen); Shu-Chin Chi(Shu-Chin Chien); Chen-Chi Lee(Chen-Chi Lee, ); Dai-Dyi Town(Dai-Dyi Town); Wen-Lin Chen(Wen-Lin Chen); L i-Feng Che(L i-Feng Chen); Meng-Shan Le(Meng-Shan Lee); ,(Chen-Wen Pan,); ,(Ku-Chien Lin,); Tze-Tien Yeh(Tze-Tien Yeh); ; ; |
中國醫藥大學 |
2014-03 |
Detection of altered methylation status at 11p15 and 7q32 in placental mesenchymal dysplasia
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陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Ming-Huei Lin);(Tao-Yeuan Wang);(Schu-Rern Chern);(Yu-Ling Kuo);(Yu-Ting Chen);(Wayseen Wang) |
中國醫藥大學 |
2014-03 |
A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation
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陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Schu-Rern Chern);(Peih-Shan Wu);蘇俊維(Jun-Wei Su);(Chen-Chi Lee);(Wayseen Wang) |
中國醫藥大學 |
2014-03 |
Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization and literature review
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陳持平(Chih-Ping Chen)*;(Liang-Kai Wang);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Yu-Ling Kuo);(Wen-Lin Chen);(Meng-Shan Lee);(Wayseen Wang) |
中國醫藥大學 |
2014-03 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET
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陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Shee-Uan Chen);(Tung-Yao Chang);(Pei-Chen Wu);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ling Kuo);(Wayseen Wang) |
中國醫藥大學 |
2014-03 |
Effect of gonadotropin-releasing hormone agonist on ES-2 ovarian cancer cells
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(Kuan-Hao Tsui);(Wen-Ling Lee,);(Kok-Min Seow);(Lin-Wei Yang);(Shih-Yi Wang);(Peng-Hui Wang)*;(Chi-Lun Chang);(Ming-Shyen Yen);(Jiin-Tsuey Cheng);陳持平(Chih-Ping Chen) |
中國醫藥大學 |
2014-03 |
Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes
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陳持平(Chih-Ping Chen)*;(Pu-Tsui Wang);(Shuan-Pei Lin);(Schu-Rern Chern);(Yu-Ting Chen);(Peih-Shan Wu);(Yu-Ling Kuo);(Wen-Lin Chen);(Wayseen Wang) |
中國醫藥大學 |
2014-03 |
Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p
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陳持平(Chih-Ping Chen)*;(Chen-Ju Lin);(Tsang-Ming Ko);(Schu-Rern Chern);(Yu-Ting Chen);(Peih-Shan Wu);(Yu-Ling Kuo);(Meng-Shan Lee);(Wayseen Wang) |
中國醫藥大學 |
2014-03 |
Directly transmitted 4.5-Mb triplication of 4q12-q13.1: prenatal diagnosis and molecular cytogenetic characterization
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陳持平(Chih-Ping Chen)*;(Ming-Huei Lin);(Schu-Rern Chern);(Yu-Ting Chen);(Peih-Shan Wu);(Yu-Ling Kuo);(Meng-Shan Lee);(Wayseen Wang) |
中國醫藥大學 |
2014-03 |
Sex ratio at a tertiary medical center in northern Taiwan – An analysis of amniocentesis
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(Ling-Chao Chen);(Chih-Yao Chen);(Huann-Cheng Horng);(Ming-Shyen Yen);(Peng-Hui Wang)*;陳持平(Chih-Ping Chen);(Wen-Hsun Chang) |