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顯示項目2851-2900 / 7244. (共145頁) << < 53 54 55 56 57 58 59 60 61 62 > >> 每頁顯示[10|25|50]項目

日期	題名	作者
2012-06	Preliminary Study of the Application of PET Knitted Fabrics in Artificial Bone Scaffold	(Ching-Wen Lou); (Mei-Hui Li); (Wen-Cheng Chen)*; (Jin-Jia Hu); (Chao-Tsang Lu); 林佳弘(Jia-Horng Lin)*
1999-03	Preliminary Study of the Voice Characteristics of Yin-vacuity Patients	楊中賢(Chung-Hsion Yang); 張恆鴻*; 邱創乾; 陳瑞照; 卓家祥; 吳文祥; 羅綸謙(Lun-Chien Lo)
2008-06	Prenatal 3-Dimensional Sonographic and MRI Findings in Omphalocele–Exstrophy–Imperforate Anus–Spinal Defects Complex.	陳持平(Chih-Ping Chen)*; 張東曜(Tung-Yao Chang); 劉育鵬(Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); 簡淑錦(Shu-Chin Chien); 曹建銘(Chien-Ming Tsao); 楊曉白(Hsiao-Bai Yang); 王偉信(Wayseen Wang)
2009-02-28	prenatal detection of a de novo satellited Yp from the father carrying a satellited Xp as a possible result of an unstable translocation during Xp-Yp pairing	簡淑錦(Shu-Chin Chien); (Cheng-Tiao Hsieh PhD); 何銘(Ming- Ho); 林齊強(Chyi-Chyang Lin); 蔡輔仁(Fuu-Jen Tsai)*
2012-09	Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); (Jun-Wei Su); (Yu-Ting Chen); (Chen-Chi Lee); (Wayseen Wang)
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)
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)
2012-03	Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review	陳持平(Chih-Ping Chen)*
2010-03	PRENATAL DIAGNOSIS AND GENETIC COUNSELING FOR MOSAIC TRISOMY 13	陳持平(Chih-Ping Chen)*
2007-03	Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome)	陳持平(Chih-Ping Chen)*; 林炫沛(Shuan-Pei Lin); 曾嶔元(Chin-Yuan Tzen); 胡務亮(Wuh-Liang Hwu); 陳樹人(Schu-Rern Chern); 莊志光(Chih-Kuang Chuang); 蔣淑清(Shu-Shien Chien); 王偉信(Wayseen Wang)
2005	Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3 -> qter) and partial trisomy 18q (18q23 -> qter) in a fetus associated with cystic hygroma and ambiguous genitalia	Chen, CP; Chern, SR; Wang, TH; Hsueh, DW; Lee, CC; Town, DD; Wang, WS; Ko, TM
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)
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)
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)
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)
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)
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)
2010-06	Prenatal diagnosis and molecular cytogenetic characterization of a small supermerary marker chromosome dericed from chromosome 18 and associated with a reciprocal translocation involving chromosome 17 and 18.	Chen)*, 陳持平(Chih-Ping; Lin), 林齊強(Chyi-Chyang
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)
2010-09	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21	陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Tsang-Ming Ko); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chen-Chi Lee); (Yu-Ting Chen); (Pei-Chen Wu); (Wayseen Wang)
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)
2010-12	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8	陳持平(Chih-Ping Chen)*; (Ming Chen); (Tsang-Ming Ko); (Gwo-Chin Ma); 蔡輔仁(Fuu-Jen Tsai); (Ming-Song Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Li-Feng Che); (Wayseen Wang)
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)
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)
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)
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)
2012-09	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2	陳持平(Chih-Ping Chen)*; (Ming Chen); (Schu-Rern Chern); (Peih-Shan Wu); (Shun-Ping Chang); (Dong-Jay Lee); (Yu-Ting Chen); (Li-Feng Chen); (Jun-Wei Su,); (Alan Hwa-Ruey Hsieh); (Alex Hwa-Jiun Hsieh); (Wayseen Wang)
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	陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); (Tung-Yao Chang); (Yi-Ning Su); (Yi-Yung Chen); (Jun-Wei Su); (Wayseen Wang)
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)
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)
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)*
2011-12	Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction	(Yi-Hui Lin); 陳持平(Chih-Ping Chen)*; (Tze-Chien Chen); (Chun-Sen Hsu); (Szu-Yuan Chou); 簡淑錦(Shu-Chin Chien)
2006	Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32->qter)and partial monosomy 21q(21q22.2->qter).	陳持平(Chen CP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,)
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)
2005	Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy	Chen, CP; Shih, JC; Chang, TY; Chern, SR; Lin, CY; Wang, WS; Tzen, CY
2012-12	Prenatal diagnosis of an interstitial deletion of 10q (10q11.21->q21.1): array comparative genomic hybridization characterization and literature review	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); (Peih-Shan Wu); (Jun-Wei Su); (Dai-Dyi Town); (Wayseen Wang)
2009-09	Prenatal diagnosis of and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly	陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Kevin Ko); (Wayseen Wang)
2009-09	Prenatal diagnosis of and molecular analysis of trisomy 13 mosaicism	陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Chen-Wen Pan); (Wayseen Wang)
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)
2007-06	Prenatal diagnosis of atypical facial clefting should alert amniotic band syndrome and prompt a search for associated amniotic bands and other structural anomalies	陳持平(Chih-Ping Chen)*
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)
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)
2005	Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes	Chen, CP; Chen, CY; Lin, CY; Shaw, SW; Wang, WS; Tzen, CY
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)
2007-09	Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies	陳持平(Chih-Ping Chen)*
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)
2005	Prenatal diagnosis of de novo partial trisomy 13q (13q22 -> qter) and partial monosomy 8p (8p23.3 -> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart	Chen, CP; Chern, SR; Hsu, CY; Lee, CC; Lee, MS; Wang, WS
2005	Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency	Chen, CP; Chern, SR; Chang, TY; Chen, WL; Chen, LF; Wang, WS; Chen, HEC
2006	Prenatal diagnosis of de novo t(2;18;14) (q33.1;q12.2; q31.2),dup(5)(q34q34), del(7)(p21.1p21.1), and del(10) (q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements	陳持平(Chen CP,); (Chern SR,); (Lee CC,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Chen WL,); (Wang W.)
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)

顯示項目2851-2900 / 7244. (共145頁) << < 53 54 55 56 57 58 59 60 61 62 > >> 每頁顯示[10|25|50]項目