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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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Date
Title
Authors
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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14
15
>
>>
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