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中國醫藥大學機構典藏 China Medical University Repository, Taiwan > 依題名瀏覽

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顯示項目20801-20850 / 54961. (共1100頁)
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日期	題名	作者
2008-09-21	The Preliminary Study on Plant Regeneration and Callus Inductio in Hypericum japonicum	李佩珊; 張婷翔; 張君儀; 李孟修(Meng-Shiou Lee); 闕甫伈; 郭昭麟(Kuo Chao-Lin)*
2008-09-21	The Preliminary Study on Plant Regeneration and Callus Induction in Hypericum japonicum.	(Pei-Shan Li); (ing-Hsaing Chang); 李孟修(Meng-Shiou Lee); (Fu-Shin Chueh); (Chao-Lin Kou.)*
2010-04	A preliminary study to evaluate a patient-centred asthma education programme on parental control of home environment and asthma signs and symptoms in children with moderate-to-severe asthma	曾麗芬(Tzeng, L. F.)、蔣立琦(Li-Chi Chiang)、薛凱中(Kai-Chung Hsueh)、馬維芬(Wei-Fen Ma)、傅令嫻(Fu, L. S.)*
2013-12-14	A preliminary study to explore the different characteristics between those elderly who used Traditional Chinese Medicine and not in Taiwan	陳奕良(Yi-Liang Chen); 林香汶(Margaret Hsiang-Wen Lin)
2009-05-02	Preliminary treatment outcome of intensity modulated radiotherapy with or without chemotherapy for nasopharyngeal carcinoma	王耀慶(Yao-Ching Wang); 楊世能(Shih-Neng Yang); 簡君儒(Chun-Ru Chien); 陳尚文(Shang-Wen Chen); 林芳仁; 郭于誠(Yu-Cheng, Kuo); 蔡銘修(Ming-Hsui Tsai); 梁基安(Ji-An Liang)*
2008-11-14	A prelusive study of minimal perceived current (MPC) measurement in healthy	黃家樂(Kar-Lok Wong); 何始生(Cheesang Ho)
2011-04	Premature aging with impaired oxidative stress defense in mice lacking TR4	(Yi-Fen Lee); (Su Liu); (Ning-Chun Liu); (Ruey-Sheng Wang); 陳璐敏(Lu-Min Chen); (Wen-Jye Lin); (Huei-Ju Ting); (Hsin-Chiu Ho,); (Gonghui Li); (Puzas EJ); (Edward J. Puzas,); (Qiao Wu,); 張傳祥*
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)
2015-04	Prenatal and Postnatal Exposure to Phthalate Esters and Asthma: A 9-Year Follow-Up Study of a Taiwanese Birth Cohort	(Hsiu Ying Ku); (Pen Hua Su); (Hui Ju Wen); (Hai Lun Sun); (Chien Jen Wang); (Hsiao Yen Chen); (Jouni J. K. Jaakkola); 王淑麗(Shu-Li Wang)*
2003	Prenatal cytogenetic detection of an unbalanced karyotype involving 9p-and 18q duplication in a fetus with apparently normal phenotype.	Lin, CC; Hsieh, LJ; Pan, YJ; Li, YC
2015-01	Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats	(Yueh-Chun Li); (Shu-Chin Chien); (Sunita R. Setlur); 林瑋德(Wei-De Lin); 蔡輔仁(Fuu-Jen Tsai); 林齊強(Chyi-Chyang Lin)*
2015-01	Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats	(Yueh-Chun Li); (Shu-Chin Chien); (Sunita R. Setlur); 林瑋德(Wei-De Lin); 蔡輔仁(Fuu-Jen Tsai); 林齊強(Chyi-Chyang Lin)*
2006-10	Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype	林齊強(Chyi-Chyang Lin); 謝耀元; (Chung-Hsing Wang); (Yueh-Chun Li); 謝麗嬌(Lie-Jiau Hsieh); 李正淳(Cheng-Chun Lee); 蔡長海(Chang-Hai Tsai); 蔡輔仁(Fuu-Jen Tsai)*
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)*
2008-03-15	prenatal detection of a maternal inherited 9q32-q33.3 deletion in a female with cleft palate	簡淑錦(Shu-Chin Chien)
2008-02-23	Prenatal Detection of Aberrant Karyotypes Using Genetic Amniocentesis:Experience from 1995 to 2007	(Shi Sue-Lin); (Lin Chyi-Chyang); (Tsai Fuu-Jen); (Chiu Tsan-Hung); (Ho Ming); (Chien Shu-Chin); 鄭如茜(Ju Chien Cheng)
2008-02-23	Prenatal Detection of Aberrant Karyotypes Using Genetic Amniocentesis:Experience from 1995 to 2007	(Shi Sue-Lin); (Lin Chyi-Chyang); (Tsai Fuu-Jen); (Chiu Tsan-Hung); (Ho Ming); (Chien Shu-Chin); 鄭如茜(Ju Chien Cheng)
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)*
2002	Prenatal diagnosis of abdominal lymphangioma	Ho, M; Lee, CC; Lin, TY
2002-08	Prenatal diagnosis of abdominal lymphangioma	何銘(Ming- Ho); 李建忠(C.C Lee); 林智一(Tze-Yi Lin)
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

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