| 中國醫藥大學 |
2011-09 |
Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review
|
陳持平(Chih-Ping Chen)*;(Ming Chen);(Yi-Ju Pan);(Yi-Ning Su);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Yu-Ting Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2011-09 |
De novo duplication Xq22.1->q24 with a disruption of the NXF geen cluster in a mentally retarded woman with short stature and premature ovarian failure
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Hung-Hung Lin);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Chen-Chi Lee);(Yu-Ting Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2011-09 |
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Yi-Yung Chen);(Schu-Rern Chern);(Yu-Peng Liu);(Pei-Chen Wu);(Chen-Chi Lee);(Yu-Ting Chen);(Wayseen Wang) |
| 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) |
| 中國醫藥大學 |
2011-09 |
Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Yu-Ting Chen);(Wen-Lin Chen);(Lee James Hsu);(Wayseen Wang) |
| 中國醫藥大學 |
2011-09 |
Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Shin-Yu Lin);(Schu-Rern Chern);(Yu-Ting Chen);(Meng-Shan Lee);(Wayseen Wang) |
| 中國醫藥大學 |
2011-09 |
Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay
|
陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Chen-Chi Lee);(Wayseen Wang) |
| 中國醫藥大學 |
2011-09 |
Prenatal diagnosis of microvillus inclusion disease
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Schu-Rern Chern);(Pei-Chen Wu);(Wayseen Wang) |
| 亞洲大學 |
2011-06 |
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p
|
陳持平;Chen, Chih-Ping;Yi-Ning Su;Schu-Rern Chern;Fuu-Jen Tsai;Pei-Chen Wu;Chen-Chi Lee;Wayseen Wang |
| 中國醫藥大學 |
2011-06 |
Rapid aneuploidy diagnosis by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal nuchal edema and mild ascites
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Pei-Chen Wu);(Chen-Chi Lee);(Chen-Wen Pan);(Wayseen Wang) |
| 中國醫藥大學 |
2011-06 |
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis
|
陳持平(Chih-Ping Chen)*;(Jui-Der Liou);(Chi-Hsin Chiang);(Yi-Ning Su);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Yu-Ting Chen);(Chen-Chi Lee);(Wen-Lin Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2011-06 |
Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Chin-Yuan Hsu);(Ming-Ren Chen);(Yu-Peng Liu);(Pei-Chen Wu);(Wayseen Wang) |
| 中國醫藥大學 |
2011-03 |
Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Meng-Shan Lee); (Wayseen Wang) |
| 中國醫藥大學 |
2011-03 |
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Shin-Yu Lin); (Chih-Long Chang); (Yeou-Lih Wang); (Jiau-Pei Huang); (Chen-Yu Chen); (Fang-Yu Hung); (Yi-Yung Chen); (Pei-Chen Wu); (Wayseen Wang) |
| 中國醫藥大學 |
2011 |
Novel heterozygous tissue-nonspecific alkaline phosphatase (TNAP) gene mutations causing lethal perinatal hypophosphatasia.
|
(Kai-Chi Chang); 林柏翰(Po-Han Lin); (Yi-Ning Su); (Steven Shinn-Forng Peng); (Ni-Chung Lee); (Hung-Chieh Chou); (Chien-Yi Chen); (Wu-Shiun Hsieh); (Po-Nien Tsao)* |
| 亞洲大學 |
2010-12 |
Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling
|
Chih-Ping Chen; Yi-Ning Su;Chin-Yuan Hsu;Schu-Rern Chern;Fuu-Jen Tsai;Pei-Chen Wu;Po-Tsang Chen;Wayseen Wang |
| 中國醫藥大學 |
2010-12 |
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
|
陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Wayseen Wang) |
| 中國醫藥大學 |
2010-12 |
Balanced reciprocal translocations at amniocentesis
|
陳持平(Chih-Ping Chen)*; (Pei-Chen Wu); (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chen-Chi Lee); (Dai-Dyi Town); (Wen-Lin Chen); (Li-Feng Chen); (Meng-Shan Lee); (Chen-Wen Pan); (Wayseen Wang) |
| 中國醫藥大學 |
2010-12 |
Partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Richard Shih-Hung Young); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Schu-Rern Chern); (Dai-Dyi Town); (Chen-Wen Pan); (Wayseen Wang) |
| 中國醫藥大學 |
2010-12 |
Partial trisomy 10q (10q25.1->qter) and partial monosomy 13q (13q34->qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Wen-Lin Chen); (Wayseen Wang) |
| 中國醫藥大學 |
2010-12 |
Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling
|
陳持平(Chih-Ping Chen)*; (Ming-Chao Huang); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Dai-Dyi Town); (Chen-Wen Pan); (Wayseen Wang) |
| 中國醫藥大學 |
2010-12 |
Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Chin-Yuan Hsu); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Po-Tsang Chen); (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 and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly
|
陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chin-Yuan Hsu); (Pei-Chen Wu); (Dai-Dyi Town); (Dong-Jay Lee); (Gwo-Chin Ma); (Wayseen Wang) |
| 中國醫藥大學 |
2010-09 |
Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization
|
陳持平(Chih-Ping Chen)*; (Yung-Ting Guo); (Shuan-Pei Lin); (Yi-Ning Su); (Yann-Jang Chen); (Rui-Yuan Hseuh); (Yi-Hui Lin); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Wayseen Wang) |
| 中國醫藥大學 |
2010-09 |
Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); (Yu-Ming Hwu); (Shuan-Pei Lin); (Chyong-Hsin Hsu); 蔡輔仁(Fuu-Jen Tsai); (Tao-Yeuan Wang); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Li-Feng Chen); (Wayseen Wang) |
| 中國醫藥大學 |
2010-09 |
Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses
|
陳持平(Chih-Ping Chen)*; (Hsien-Ming Lin); (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Meng-Shan Lee); (Chen-Wen Pan); (Wayseen Wang) |
| 中國醫藥大學 |
2010-09 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22
|
陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chen-Chi Lee); (Wen-Ling Chen); (Li-Feng Chen); (Pei-Chen Wu); (Wayseen Wang) |
| 中國醫藥大學 |
2010-06 |
Apert syndrome associated with upper airway obstruction and gastroesophageal reflux presenting polyhydramnios in the third trimester
|
陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); (Yi-Ning Su); (Chen-Yu Chen); 蔡輔仁(Fuu-Jen Tsai); (Yu-Peng Liu); (Schu-Rern Chern); (Pei-Chen Wu); (Hsaio-En Cindy Chen); (Wayseen Wang) |
| 中國醫藥大學 |
2010-06 |
Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Hsaio-En Cindy Chen); (Shu-Shien Chiang); (Wayseen Wang) |
| 中國醫藥大學 |
2010-06 |
Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Jon-Kway Huang); (Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); (Chun-Kuang Yang); (Jian-Pei Huang); (Chen-Yu Chen); (Pei-Chen Wu); (Wayseen Wang) |
| 中國醫藥大學 |
2010-03 |
Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array CGH in pregnancy with abnormal ultrasound findings detected in late second and third trimesters
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chin-Yuan Hsu); (Ming-Chao Huang); (Wayseen Wang) |
| 中國醫藥大學 |
2010-03 |
Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Chin-Yuan Hsu); (Pei-Ying Ling); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Hsaio-En Cindy Chen); (Wayseen Wang) |
| 中國醫藥大學 |
2010-03 |
Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome.
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); 簡淑錦(Shu-Chin Chien) |
| 中國醫藥大學 |
2010-03 |
Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Chen-Chi Lee); (Wayseen Wang) |
| 中國醫藥大學 |
2010-02 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18
|
陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Yu-Ting Chen); (Schu-Rern Chern); (Chen-Chi Lee); (Dai-Dyi Town); (Li-Feng Chen); (Pei-Chen Wu); (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 terminal 2q deletion and distal 15q duplication by array comparative genomic hybridization using uncultured amniocytes
|
陳持平(Chih-Ping Chen)*; (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Schu-Rern Chern); (Meng-Shan Lee); (Jonathan Kwei Hwang); (Teresa Hsiao-Tien Chen); (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 |
2008-06 |
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation.
|
陳持平(Chih-Ping Chen); (Shuan-Pei Lin); (Yi-Ning Su); 簡淑錦(Shu-Chin Chien); 蔡輔仁(Fuu-Jen Tsai); (Wayseen Wang) |
| 中國醫藥大學 |
2007-12 |
Genetic counseling of prenatally detected unbalanced t(Y;15)(q12;p13)
|
陳持平(Chih-Ping Chen); (Yi-Ning Su); (Chyi-Chyang Lin); (Yueh-Chun Li); (Lie-Jiau Hsieh); (Chen-Chi Lee); (Wayseen Wang) |
