| 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 |
2015-02 |
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 |
2014-06 |
Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects
|
Yu-Ling Kuo;Chih-Ping Chen;Liang-Kai Wang;Tsang-Ming Ko;Tung-Yao Chang;Schu-Rern Chern;Peih-Shan Wu;Yu-Ting Chen;Shu-Yuan Chang |
| 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 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET
|
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 |
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 |
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 |
2013-04 |
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization
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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 |
2012-06 |
Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene
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陳持平(Chih-Ping Chen)*;(Schu-Rern Chern);(Tung-Yao Chang);(Yi-Ning Su);(Yi-Yung Chen);(Jun-Wei Su);(Wayseen Wang) |
| 中國醫藥大學 |
2012-06 |
Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the asymptomatic father
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陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Tung-Yao Chang);(Schu-Rern Chern);(Chen-Yu Chen);(Jun-Wei Su);(Wayseen Wang) |
| 中國醫藥大學 |
2012-06 |
Identification of a deletion mutation in the short flanking repeat region of exon 44 of COL1A1 gene in a fetus with osteogenesis imperfecta type II
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陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Tung-Yao Chang);(Schu-Rern Chern);(Jun-Wei Su);(Wayseen Wang) |
| 中國醫藥大學 |
2012-06 |
Osteogenesis imperfecta type II: prenatal diagnosis and association with increased nuchal translucency and hypoechogenicity of the cranium
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Tung-Yao Chang);(Ming-Chao Huang);(Chun-Heng Pan);(Schu-Rern Chern);(Jun-Wei Su);(Wayseen Wang) |
| 中國醫藥大學 |
2012-04 |
Persistent cloaca presenting with a perineal cyst: prenatal ultrasound and magnetic resonance imaging findings
|
陳持平(Chih-Ping Chen)*;(Tung-Yao Chang);(Chin-Yuan Hsu);(Yu-Peng Liu);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Wayseen Wang) |
| 中國醫藥大學 |
2012-03 |
Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular genetic analysis
|
陳持平(Chih-Ping Chen)*;(Tung-Yao Chang);(Tao-Yeuan Wang);(Chen-Yu Chen);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Schu-Rern Chern);(Wayseen Wang) |
| 中國醫藥大學 |
2011-12 |
Perinatal magnetic resonance imaging demonstration of duplication of the right renal collecting system with ipsilateral hydronephrosis and hydroureter, and contralateral renal hypoplasia
|
陳持平(Chih-Ping Chen)*;(Jeng-Daw Tsai);(Chin-Yuan Hsu);(Tung-Yao Chang);(Yu-Peng Liu);(Jun-Wei Su);(Wayseen Wang) |
| 中國醫藥大學 |
2010-09 |
Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Tung-Yao Chang); (Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); (Ming-Ren Chen); (Jonathan Kwei Hwang); (Teresa Hsiao-Tien Chen); (Wayseen Wang) |
| 中國醫藥大學 |
2010-09 |
Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy
|
陳持平(Chih-Ping Chen)*; (Yu-Peng Liu); (Tung-Yao Chang); 蔡輔仁(Fuu-Jen Tsai); (Chen-Yu Chen); (Pei-Chen Wu); (Teresa Hsiao-Tien Chen); (Wayseen Wang) |
| 亞洲大學 |
2009-12 |
22q 11.2 Microdeletion in a Fetus With Double-outlet Right Ventricle, Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis by Array Comparative Genomic Hybridization
|
Chih-Ping Chen;Yi-Ning Su;Tung-Yao Chang;Schu-Rern Chern;Fuu-Jen Tsai;Jonathan Kwei Hwang;Wayseen Wang; |
| 中國醫藥大學 |
2009-12 |
22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect by array comparative genomic hybridization
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Tung-Yao Chang); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Jonathan Kwei Hwang); (Wayseen Wang) |
| 中國醫藥大學 |
2009-12 |
Prenatal diagnosis of monosomy 17p (17p13.3->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly and Miller-Dieker lissencephaly syndrome in a fetus
|
(Chin-Yi Lin); 陳持平(Chih-Ping Chen)*; (Chiung-Ling Liau); (Pen-Hua Su); (Teng-Fu Tsao); (Tung-Yao Chang); (Wayseen Wang) |
| 中國醫藥大學 |
2009-09 |
Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Tung-Yao Chang); (Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); (Jonathan Kwei Hwang); (Wayseen Wang) |
| 中國醫藥大學 |
2009-03 |
Prenatal diagnosis of 46,XX,der(13;21)(q10;q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites
|
陳持平(Chih-Ping Chen); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Tung-Yao Chang); (Chin-Yuan Hsu); (Hung-Hung Lin); (Wayseen Wang) |
| 中國醫藥大學 |
2008-05 |
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand foot malformation associated with partial monosomy 4p (4p16.1->pter) and partial trisomy 10q (10q25.1->qter)
|
陳持平(Chih-Ping Chen); (Yann-Jang Chen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Tung-Yao Chang); (Chen-Chi Lee); (Dai-Dyi Town); (Meng-Shan Lee); (Wayseen Wang) |
| 亞洲大學 |
2008-03 |
PRENATAL SONOGRAPHIC AND MAGNETIC RESONANCE IMAGING DEMONSTRATION OF A RIGHT MIDLINE ARACHNOID CYST ASSOCIATED WITH VENTRICULOMEGALY, COLPOCEPHALY, DILATION OF THE THIRD VENTRICLE, ABSENCE OF CAVUM SEPTI PELLUCIDI, AGENESIS OF THE CORPUS CALLOSUM AND MEGA Cisterna Magna
|
Chih-Ping Chen;Tung-Yao Chang;Jeng-Hsiu Hung;Chen-Yu Chen;Wayseen Wang |
| 中國醫藥大學 |
2008-03 |
Prenatal evaluation of a giant blind ectopic ureter associated with a duplex kidney with magnetic resonance imaging.
|
陳持平(Chih-Ping Chen); (Yu-Peng Liu); (Jian-Pei Huang); (Tung-Yao Chang); 蔡輔仁(Fuu-Jen Tsai); (Jeng-DauTsai); (Jin-Cherng Sheu); (Wayseen Wang) |
| 中國醫藥大學 |
2008-03 |
Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy
|
陳持平(Chih-Ping Chen)*; (Tung-Yao Chang); (Hung-Hung Lin); (Schu-Rern Chern); (Wayseen Wang) |
| 中國醫藥大學 |
2008-03 |
Prenatal sonographic and magnetic resonance imaging demonstration of a right midline arachnoid cyst associated with ventriculomegaly, colpocephaly, dilation of the third ventricle, absence of cavum septi pellucidum, agenesis of the corpus callosum and meg
|
陳持平(Chih-Ping Chen); (Tung-Yao Chang); (Jeng-Hsiu Hung); (Chen-Yu Chen); (Wayseen Wang) |
| 中國醫藥大學 |
2007-12 |
Abnormal prenatal hematological findings in congenital leukemia of Down syndrome with hepatosplenomegaly
|
陳持平(Chih-Ping Chen); (Shuan-Pei Lin); (Tung-Yao Chang); (Hsin-Tsung Ho) |
