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Introduction: 馬偕醫學院生物醫學研究所於民國101年成立並開始招生。


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Showing items 251-275 of 499. (20 Page(s) Totally)
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DateTitleAuthors
2011-12-01 Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Schu-Rern Chern; Chen-Chi Lee; Yu-Ting Chen; Wen-Lin Chen; Wayseen Wang
2012-12-01 Mosaic isochromosome 20q detected at amniocentesis may be a cell culture artifact Chih-Ping Chen; Shuenn-Dyh Chang; Yu-Ting Chen; Jun-Wei Su; Dai-Dyi Town; Wayseen Wang
2010-09-01 Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and dsomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization 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
2012-03-01 Mosaic ring chromosome 21, monosomy 21 and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3 Chih-Ping Chen; Yi-Hui Lin; Szu-Yuan Chou; Yi-Ning Su; Schu-Rern Chern; Yu-Ting Chen; Dai-Dyi Town; Wen-Lin Chen; Chen-Wen Pan; Wayseen Wang
2011-09-01 Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Wayseen Wang
2011-09-01 Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses Chih-Ping Chen; Shuan-Pei Lin; Ming Chen; Yi-Ning Su; Schu-Rern Chern,; Tao-Yeuan Wang; Yu-Peng Liu; Fuu-Jen Tsai; Chen-Chi Lee; Yen-Jiun Chen; Wayseen Wang
2010-06-01 Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Hsaio-En Cindy Chen; Shu-Shien Chiang; Wayseen Wang
2012-12-01 Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Yu-Ting Chen; Peih-Shan Wu; Jun-Wei Su; Chen-Wen Pan; Wayseen Wang
2010-09-01 Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Yu-Ming Hwu; Shuan-Pei Lin; Chyong-Hsin Hsu; Fuu-Jen Tsai; Tao-Yeuan Wang; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Li-Feng Chen; Wayseen Wang
2010-09-01 Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses Chih-Ping Chen; Hsien-Ming Lin; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
2008-01-01 Mothers’ experience supporting life adjustment in children with T1DM. Lin HP; Mu PF; Lee YJ
2011-02-01 MUC4 gene polymorphisms associate with endometriosis development and endometriosis-related infertility Cherry Yin-Yi Chang; Hui-Wen Chang; Chih-Mei Chen; Chia-Ying Lin; Chih-Ping Chen; Chih-Ho Lai; Wei-Yong Lin; Hsing-Ping Liu; Jim Jinn-Chyuan Sheu; Fuu-Jen Tsai
2001-07-01 Multiple endocrine neoplasia 2B (MEN 2B) Lee YJ; Liu HC; Lee HC; Tzen CY; Huang CY; Yang TL
2009-11-01 Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome Chia-Cheng Hung; Shin-Yu Lin; Chien-Nan Lee; Hui-Yu Cheng; Shuan-Pei Lin; Ming-Ren Chen; Chih-Ping Chen; Chien-Hui Chang; Chiou-Ya Lin; Chih-Chieh Yu; Hsin-Hui Chiu,; Wen-Fang Cheng; Hong-Nerng Ho; Dau-Ming Niu; Yi-Ning Su
2007-01-01 Mutational Analysis of PTPN11 Gene in Taiwanese Children with Noonan Syndrome. Hung CS; Lin JL; Lee YJ; Lin SP; Chao MC; Lo FS
2014-03-01 Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic Chinese Wu YL; Hwang DW; Hsiao HP; Ting WH; Huang CY; Tsai WY; Chen HC; Chao MC; Lo FS; Tsai JD; Yang S; Shih SL; Lin CL; Lee YJ
2007-05-01 Neck abscess and necrotizing fasciitis caused by Salmonella infection: a report of 2 cases. Luo CW; Liu CJ
2000-06-01 Neonatal adrenal hemorrhage Huang CY; Lee YJ; Lee HC; Huang FY
2002-06-01 Neonatal adrenal hemorrhage: 4-year experience Chang HY; Yeung CY; Hsu CH; Lee HC; Lee YJ; Lin DS; Lin CC
2012-12-01 Neural Stem Cells and Cell-based Approaches in Neurodegeneration and Peripheral Nerve Injuries Hsu YC; Chiu IM
1995-04-01 Neurogenic diabetes insipidus in a child with fatal Coxsackie virus B1 encephalitis ann-Jinn Lee; Dine Yang; Shyh-Dar Shyur; Nan-Chang Chiu
1996-03-01 Neurogenic diabetes insipidus in children with hypoxic encephalopathy Lee YJ; Huang FY; Shen EY; Kao HA; Ho MY; Shyur SD; Chiu NC
2013-08-01 The new face of the old molecules: crustin Pm4 and transglutaminase type I serving as rnps down-regulate astakine-mediated hematopoiesis Yun-Tsan Chang; Cheng-Yung Lin; Che-Yiang Tsai; Vinu S Siva; Chia-Ying Chu; Huai-Jen Tsai; Yen-Ling Song
2001-02-01 Newborns with ambiguous genitalia, impalpable gonads, and hyperpigmentation Chang HY; Lee YJ; Lin SP; Lee HH
2008-04-01 NFkB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1→qter) Chih-Ping Chen; Yann-Jang Chen; Fuu-Jen Tsai; Schu-Rern Chern; Wayseen Wang

Showing items 251-275 of 499. (20 Page(s) Totally)
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