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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 76-100 of 499. (20 Page(s) Totally)
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DateTitleAuthors
2007-06-01 Comparison of one-tube multiplex PCR and automated ribotyping for rapid identification of Acinetobacter baumannii. Chen, T. L., Siu, L. K., Wu, R. C. C., Shaio, M. F., Hua;
2009-09-01 Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review Chih-Ping Chen; Yu-Peng Liu; Fuu-Jen Tsai; Chen-Yu Chen; Hung-Hung Lin; Pei-Chen Wu; Wayseen Wang
2008-12-01 Concomitant exencepahly and limb defects associated with pentalogy of Cantrell Chih-Ping Chen; Chin-Yuan Tzen; Chen-Yu Chen; Fuu-Jen Tsai; Wayseen Wang
2008-03-01 Concomitant occurrence of holoprosencephaly and omphalocele Chih-Ping Chen.;
2008-03-01 Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy Chih-Ping Chen; Tung-Yao Chang; Hung-Hung Lin; Schu-Rern Chern; Wayseen Wang
1998-06-01 Congenital nasal pyriform aperture stenosis and solitary maxillary central incisor Lo FS; Lee YJ; Lin SP; Shen EY; Huang JK; Lee KS
1999-02-01 Congenital nasal pyriform aperture stenosis: A diagnostic clue to solitary maxillary central incisor prior to eruption in three infants Fu-Sung Lo; Kuo-Sheng Lee; Lih-Sheng Chen; Han-Yang Hung; Chyong-Hsin Hsu; Shuan-Pei Lin; Yann-Jinn Lee
1997-04-01 Congenital rickets - A patient report Wang LY; Hung HY; Hsu CH; Shih SL; Lee YJ
2011-03-01 Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Schu-Rern Chern; Pei-Chen Wu; Chen-Chi Lee; Meng-Shan Lee; Yu-Ting Chen; Wayseen Wang
2011-12-01 Conjoined twins detected in the first trimester: a review Chih-Ping Chen; Chin-Yuan Hsu; Jun-Wei Su; Hsiao-En Cindy Chen; Alan Hwa-Ruey Hsieh; Alex Hwa-Jiun Hsieh; Wayseen Wang
2007-06-01 Construction and characterization of an expressed sequenced tag library for the mosquito vector Armigeres subalbatus George F. Mayhew, Lyric C. Bartholomay, Hang-Yen Kou, Th;
1995-04-01 Continuous infusion of vasopressin in comatose children with neurogenic diabetes insipidus Lee YJ; Shen EY; Huang FY; Kao HA; Shyur SD
2010-06-01 Contribution of a plasmid-borne blaOXA-58 gene with its hybrid promoter provided by IS1006 and an ISAba3-like element to beta-lactam resistance in acinetobacter genomic species 13TU. Chen TL, Chang WC, Kuo SC, Lee YT, Chen CP, Siu LK, Cho ;
2008-06-01 Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Shu-Chin Chien; Fuu-Jen Tsai; Wayseen Wang
2006-05-01 The critical roles of polyamines in regulating ColE7 production and restricting ColE7 uptake of the colicin-producing Escherichia coli. Yi-Hsuan Pan; Chen-Chung Liao; Chou-Chiang Kuo; Kow-Jen Duan; Po-Huang Liang; Hanna S. Yuan; Shiau-Ting Hu; Kin-Fu Chak
2008-01-01 Crystal structure of Escherichia coli PNPase: central channel residues are involved in processive RNA degradation. Zhonghao Shi; Wei-Zen Yang; Sue Lin-Chao; Kin-Fu Chak; Hanna S. Yuan
2007-01-01 CTLA-4 gene and susceptibility to human papillomavirus 16-associated cervical squamous cell carcinoma in Taiwanese women. Su TH; Chang TY; Lee YJ; Chen CK; Liu HF; Chu CC; Lin M; Wang PT; Huang WC; Chen TC; Yang YC
2011-06-01 Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis Chih-Ping Chen; Jui-Der Liou; Chi-Hsin Chiang,; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Yu-Ting Chen; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
2007-12-01 Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p Chih-Ping Chen; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang
2012-11-01 A de novo 4.4-Mb microdeletion in 2p24.3->p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Peih-Shan Wu; Shuenn-Dyh Chang; Shu-Hang Ng; Yu-Peng Liu; Jun-Wei Su; Wayseen Wang
2010-09-01 A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay atopic dermatitis and abnormal immunological findings Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wayseen Wang
2011-12-01 A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings Chih-Ping Chen; Hsu-Kuaing Huang; Pei-Ying Lin; Yi-Ning Su; Ming Chen; Fuu-Jen Tsai; Pei-Chen Wu; Schu-Rern Chern; Yu-Ting Chen; Chen-Chi Lee; Wayseen Wang
2011-09-01 De novo duplication Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure Chih-Ping Chen; Yi-Ning Su; Hung-Hung Lin; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wayseen Wang
2012-12-01 De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delay Chih-Ping Chen; Shuan-Pei Lin; Yuan-Ling Huang; Schu-Rern Chern; Yu-Peng Liu; Jun-Wei Su; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
2012-06-01 A de novo supernumerary marker chromosome derived from chromosome 9p (9p13.1->p23) associated with attention deficit and hyperactivity disorder Chih-Ping Chen; Shuan-Pei Lin; Jun-Wei Su; Dai-Dyi Town; Wayseen Wang

Showing items 76-100 of 499. (20 Page(s) Totally)
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