| 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) |
| 中國醫藥大學 |
2015-10 |
Interphase fluorescence in situ hybridization assisting in prenatal counseling for amniocentesis karyotyping-detected fetal mosaicism
|
(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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
(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
|
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
|
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
|
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
|
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
|
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
|
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
|
(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
|
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
|
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
|
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
|
(Ling-Chao Chen);(Chih-Yao Chen);(Huann-Cheng Horng);(Ming-Shyen Yen);(Peng-Hui Wang)*;陳持平(Chih-Ping Chen);(Wen-Hsun Chang) |
| 中國醫藥大學 |
2014-03 |
Chromosomal deletions detected at amniocentesis
|
(Chen-Ju Lin)*;陳持平(Chih-Ping Chen);簡淑錦(Shu-Chin Chien);(Chen-Chi Lee);(Dai-Dyi Town);(Wen-Lin Chen);(L i-Feng Chen);(Meng-Shan Lee);(Chen-Wen Pan);(Ku-Chien Lin);(Tze-Tien Yeh) |
| 中國醫藥大學 |
2014-03 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15
|
陳持平(Chih-Ping Chen)*;(Ming Chen);(Yi-Ning Su);(Schu-Rern Chern);(Peih-Shan Wu);(Shun-Ping Chang);(Yu-Ling Kuo);(Wen-Lin Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2013-12 |
Prenatal diagnosis of de novo cryptic microdeletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect
|
陳持平(Chih-Ping Chen)*;(Ming-Chao Huang);(Yi-Yung Chen);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Jun-Wei Su);(Wayseen Wang) |
| 中國醫藥大學 |
2013-12 |
Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review
|
陳持平(Chih-Ping Chen)*;(Tung-Yao Chang);(Wan-Yuo Guo);(Pei-Chen Wu);(Liang-Kai Wang);(Schu-Rern Chern);(Peih-Shan Wu);蘇俊維(Jun-Wei Su);(Yu-Ting Chen);(Li-Feng Chen);(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) |
| 中國醫藥大學 |
2013-12 |
3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization
|
陳持平(Chih-Ping Chen)*;(Chen-Ju Lin);(Yi-Yung Chen);(Liang-Kai Wang);(Schu-Rern Chern);(Peih-Shan Wu);蘇俊維(Jun-Wei Su);(Li-Feng Chen);(Dai-Dyi Town);(Chen-Wen Pan);(Wayseen Wang) |
| 中國醫藥大學 |
2013-07 |
6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia, psychomotor developmental delay and poor wound healing
|
陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yu-Peng Liu);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Jun-Wei Su);(Chen-Chi Lee);(Wayseen Wang) |
| 中國醫藥大學 |
2013-07 |
Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: prenatal diagnosis and aCGH characterization using uncultured amniocytes
|
陳持平(Chih-Ping Chen)*;(Ming-Chao Huang);(Yi-Yung Chen);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Jun-Wei Su);(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) |
| 中國醫藥大學 |
2013-06 |
Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review
|
陳持平(Chih-Ping Chen)*;(Po-Jen Cheng);(Shuenn-Dyh Chang);(Yi-Xuan Lee);(Jin-Chung Shih);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Adam Hwa-Ming Hsieh);(Teresa Hsiao-Tien Chen);(Li-Feng Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2013-06 |
A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene
|
陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Wayseen Wang) |
| 中國醫藥大學 |
2013-04 |
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization
|
陳持平(Chih-Ping Chen)*;(Chen-Ju Lin);(Tung-Yao Chang);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Jun-Wei Su);(Chen-Chi Lee);(Li-Feng Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis of partial trisomy 3q (3q27.3->qter) and partial monosomy 14q (14q31.3->qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints
|
陳持平(Chih-Ping Chen)*;(Yao-Lung Chang);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Wen-Lin Chen);(Li-Feng Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21->qter) and partial monosomy 6q (6q27->qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold
|
陳持平(Chih-Ping Chen)*;(Yi-Yung Chen);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Yu-Ting Chen);(Li-Feng Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2013-03 |
Incidental detection of thoracoomphalopagus at amniocentesis in a twin pregnancy
|
陳持平(Chih-Ping Chen)*;(Jun-Wei Su);(Chia-Heng Lee);(Wayseen Wang) |
| 中國醫藥大學 |
2013-03 |
Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Jun-Wei Su);(Schu-Rern Chern);(Yu-Ting Chen);(Li-Feng Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2013-03 |
Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma and intrauterine growth restriction
|
陳持平(Chih-Ping Chen)*;(Chin-Yuan Hsu);(Yi-Ning Su);(Tao-Yeuan Wang);(Yi-Yung Chen);(Schu-Rern Chern);(Jun-Wei Su);(Wayseen Wang) |
| 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) |
| 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) |
| 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 |
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) |
| 中國醫藥大學 |
2013-03 |
Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20
|
陳持平(Chih-Ping Chen)*;(Shuenn-Dyh Chang);(Ho-Yen Chueh);(Yi-Ning Su);(Schu-Rern Chern);(Jun-Wei Su);(Yu-Ting Chen);(Li-Feng Chen);(Meng-Shan Lee);(Wayseen Wang) |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism
|
陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);(Schu-Rern Chern);(Jun-Wei Su);(Wayseen Wang) |
| 中國醫藥大學 |
2013-01 |
Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosome
|
陳持平(Chih-Ping Chen)*;(Ming Chen);(Gwo-Chin Ma);(Yi-Ning Su);(Tsang-Ming Ko);(Yi-Hui Lin);(Wayseen Wang) |
| 中國醫藥大學 |
2012-12 |
Partial trisomy 1q (1q42.13->qter) and partial monosomy 6q (6q27->qter) in a girl with single median maxillary central incisor, dysgenesis of corpus callosum and developmental delay
|
陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);(Schu-Rern Chern);(Jun-Wei Su);(Chen-Chi Lee);(Wayseen Wang) |
