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Showing items 1-33 of 33  (1 Page(s) Totally)
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Institution Date Title Author
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 2015-02 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)
亞洲大學 2014-03 Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization and literature review Chih-Ping Chen;Liang-Kai Wang;Schu-Rern Chern;Peih-Shan Wug, Yu-Ting Chen;Yu-Ling Kuo;Wen-Lin Chen;Meng-Shan Lee;Wayseen Wang
亞洲大學 2014-03 Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p Chih-Ping Chen;Chen-Li 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 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 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 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)
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 2013-03 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 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)
亞洲大學 2012-09 Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes 陳持平;Chen, Chih-Ping;Dai-Dyi Town, ;Wen-Lin Chen, ;Chen, Li-Feng;Meng-Shan Lee, ;Pan, Chen-Wen;Wang, Wayseen
中國醫藥大學 2012-09 Partial monosomy 3p (3p26.2->pter) and partial trisomy 5q (5q34->qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Ming-Ren Chen);(Yi-Ning Su);(Schu-Rern Chern);(Yu-Peng Liu);(Jun-Wei Su);(Meng-Shan Lee);(Wayseen Wang)
中國醫藥大學 2012-09 Rapid diagnosis of trisomy 18 using uncultured amniocytes in late second trimester in a pregnancy with fetal congenital heart defects, arthrogryposis, omphalocele and mega cisterna magna 陳持平(Chih-Ping Chen)*;Yi-Yung Chen;(Jui-Der Liou);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Meng-Shan Lee);(Wayseen Wang)
中國醫藥大學 2012-09 Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase FISH, QF-PCR and aCGH on uncultured amniocytes in a pregnancy with fetal pyelectasis 陳持平(Chih-Ping Chen)*;(Shuenn-Dyh Chang);(Yi-Ning Su);(Ming Chen);(Schu-Rern Chern);(Jun-Wei Su);(Yu-Ting Chen);(Wen-Lin Chen,);(Chen-Wen Pan);(Meng-Shan Lee);(Wayseen Wang)
中國醫藥大學 2012-09 Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes 陳持平(Chih-Ping Chen)*;(Shuenn-Dyh Chang);(Ho-Yen Chueh);(Yi-Ning Su);(Jun-Wei Su);(Schu-Rern Chern);(Yu-Ting Chen);(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 2012-06 Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Ming-Ren Chen);(Jun-Wei Su);(Schu-Rern Chern);(Yen-Jiun Chen);(Meng-Shan Lee);(Wayseen Wang)
中國醫藥大學 2012-06 Phenotypic features associated with mosaic tetrasomy 9p in a 20-year-old female patient include autism spectrum disorder 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Jun-Wei Su);(Meng-Shan Lee);(Wayseen Wang)
中國醫藥大學 2012-03 Rapid aneuploidy diagnosis of partial trisomy 7q (7q34->qter) and partial monosomy 10q (10q26.12->qter) by array comparative genomic hybridization using uncultured amniocytes 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Dai-Dyi Town);(Li-Feng Chen);(Meng-Shan Lee);(Wayseen Wang)
中國醫藥大學 2011-12 Pure interstitial duplication of chromosome 7q (7q31.2->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and mental retardation 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Meng-Shan Lee);(Yen-Jiun Chen);(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 2011-03 Unbalanced reciprocal translocations at amniocentesis 陳持平(Chih-Ping Chen)*; (Pei-Chen Wu); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Dai-Dyi Town); (Wen-Lin Chen); (Li-Feng Chen); (Meng-Shan Lee); (Chen-Wen Pan); (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 Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome 陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Meng-Shan Lee); (Yu-Ting Chen); (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 2010-09 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 2010-06 Deletion 2q37.3->qter and duplication 15q24.3->qter characterized by array CGH in a girl with epilepsy and dysmorphic features 陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Li-Feng Chen); (Meng-Shan Lee); (Wayseen Wang)
中國醫藥大學 2010-03 UNBALANCED AND BALANCED HETEROLOGOUS ACROCENTRIC REARRANGEMENTS INVOLVING CHROMOSOME 21 AT AMNIOCENTESIS 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); (Pei-Chen Wu); 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 2009-12 Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); (Pei-Chen Wu); 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 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 2009-01 A 12 Mb deletion of 6p24.1->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys. 陳持平(Chih-Ping Chen)*; (Chin-Yuan Tzen); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Chen-Chi Lee); (Meng-Shan Lee); (Chen-Wen Pan); (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)

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