English  |  正體中文  |  简体中文  |  Items with full text/Total items : 90453/105671 (86%)
Visitors : 16045614      Online Users : 98
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
    •  Adv. Search
    Home ‧ Login ‧ Upload ‧ Help ‧ About ‧ Administer Goto mobile version

    Category

    Loading community tree, please wait....

    Year

    Loading year class tree, please wait....

    Items for Author "Chih-Ping Chen" 

    Return to Browse by Author

    Showing 40 items.

    Collection Date Title Authors Bitstream
    [國際企業學系] 期刊論文 2014-03 A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Chen-Chi Lee; Wayseen Wang
    [國際企業學系] 期刊論文 2014-03 Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization and literature review Chih-Ping Chen; Liang-Kai Wang; Schu-Rern Chern; Peih-Shan Wug, Yu-Ting Chen; Yu-Ling Kuo; Wen-Lin Chen; Meng-Shan Lee; Wayseen Wang
    [國際企業學系] 期刊論文 2014-03 Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET Chih-Ping Chen; Yi-Ning Su; Shee-Uan Chen; Tung-Yao Chang; Pei-Chen Wu; Schu-Rern Chern; Peih-Shan Wu; Yu-Ling Kuo; Wayseen Wang
    [國際企業學系] 期刊論文 2014-03 Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes Chih-Ping Chen; Pu-Tsui Wang; Shuan-Pei Lin; Schu-Rern Chern; Yu-Ting Chen; Peih-Shan Wu; Yu-Ling Kuo; Wen-Lin Chen; Wayseen Wang
    [國際企業學系] 期刊論文 2014-03 Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p Chih-Ping Chen; Chen-Li Lin; Tsang-Ming Ko; Schu-Rern Chern; Yu-Ting Chen; Peih-Shan Wu; Yu-Ling Kuo; Meng-Shan Lee; Wayseen Wang
    [國際企業學系] 期刊論文 2014-03 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15 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
    [國際企業學系] 期刊論文 2014-02 Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry Chih-Ping Chen; Ming Chen; Chen-Yu Chen; Schu-Rern Chern; Peih-Shan Wu; Shun-Ping Chang; Yu-Ling Kuo; Wen-Lin Chen; Chen-Wen Pan; Wayseen Wang
    [生物科技學系] 期刊論文 2017-08 Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect 陳持平; Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Chen-Chi Lee; Chien-Wen Ya; Chien-Wen Yang; Wayseen Wang
    [生物科技學系] 期刊論文 2017-08 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16 陳持平; Chih-Ping Chen; Tsang-Ming K; Tsang-Ming Ko; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Chien-Wen Ya; Chien-Wen Yang; Chen-Wen Pan; Wayseen Wang
    [生物科技學系] 期刊論文 2017-08 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review 陳持平; Chih-Ping Chen; Ming Chen; Chia-Hsun Wu; Chen-Ju Lin; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Shun-Ping Ch; Shun-Ping Chang; Li-Feng Chen; Wayseen Wang
    [生物科技學系] 期刊論文 2017-08 Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome 陳持平; Chih-Ping Chen; Jian-Pei Hua; Jian-Pei Huang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Chen-Chi Lee; Chien-Wen Ya; Chien-Wen Yang; Wayseen Wang
    [生物科技學系] 期刊論文 2017-08 Prenatal diagnosis of congenital lobar fluid overload Pei-Shan Tsa; Pei-Shan Tsai,; 陳持平; Chih-Ping Chen; Dao Chen Lin; Yu-Peng Liu
    [生物科技學系] 期刊論文 2017-08 Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9 陳持平; Chih-Ping Chen; Ming Chen; Liang-Kai Wa; Liang-Kai Wang; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Shun-Ping Ch; Shun-Ping Chang; Chien-Wen Ya; Chien-Wen Yang; Chen-Wen Pan; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1 陳持平; Chih-Ping Chen; Hoi-Kin Yip; Liang-Kai Wa; Liang-Kai Wang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p ；20p12-p13 encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome 陳持平; Chih-Ping Chen; Chang-Sheng; Chang-Sheng Yin; Liang-Kai Wa; Liang-Kai Wang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Wen-Lin Chen; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11 陳持平; Chih-Ping Chen; Ming Chen; Pu-Tsui Wang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Shun-Ping Ch; Shun-Ping Chang; Chen-Wen Pan; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q ；2q31.1-q32.1 encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency 陳持平; Chih-Ping Chen; Chen-Ju Lin; Yen-Ni Chen; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Li-Feng Chen; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions 陳持平; Chih-Ping Chen; Ming Chen; Yuh-Ming Hwu; Shun-Ping Ch; Shun-Ping Chang; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Chen-Chi Lee; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia 陳持平; Chih-Ping Chen; Shuan-Pei Li; Shuan-Pei Lin; Yu-Peng Liu; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Wayseen Wang
    [生物科技學系] 期刊論文 2017-04 Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis 陳持平; Chih-Ping Chen; Kuo-Gon Wang; Hsu-Kuang Hu; Hsu-Kuang Huang; Cheng-Ran Pe; Cheng-Ran Peng; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Chen-Chi Lee; Wayseen Wang
    [生物科技學系] 期刊論文 2017-04 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2 陳持平; Chih-Ping Chen; Ming Chen; Shun-Ping Ch; Shun-Ping Chang; Fang-Yu Hung; Meng-Ju Lee; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Chen; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Le; Meng-Shan Lee; Wen-Lin Chen; Wayseen Wang
    [生物科技學系] 期刊論文 2017-04 Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome 陳持平; Chih-Ping Chen; Chen-Ju Lin; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Chen-Wen Pan; Chien-Wen Ya; Chien-Wen Yang; Wayseen Wang
    [生物科技學系] 期刊論文 2017-04 Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome 陳持平; Chih-Ping Chen; Tsang-Ming K; Tsang-Ming Ko; Liang-Kai Wa; Liang-Kai Wang; Shuan-Pei Li; Shuan-Pei Lin; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Meng-Shan Le; Meng-Shan Lee; Wayseen Wang
    [生物科技學系] 期刊論文 2017-04 Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome 陳持平; Chih-Ping Chen; Fang-Yu Hung; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Chien-Wen Ya; Chien-Wen Yang; Wen-Lin Chen; Wayseen Wang
    [生物科技學系] 期刊論文 2017-04 Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q ；4q11.1-q13.2 and 5q13.2 microdeletion with no apparent phenotypic abnormality 陳持平; Chih-Ping Chen; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Chien-Wen Ya; Chien-Wen Yang; Chen-Chi Lee; Meng-Shan Le; Meng-Shan Lee
    [生物科技學系] 期刊論文 2014-06 Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects Yu-Ling Kuo; Chih-Ping Chen; Liang-Kai Wang; Tsang-Ming Ko; Tung-Yao Chang; Schu-Rern Chern; Peih-Shan Wu; Yu-Ting Chen; Shu-Yuan Chang
    [生物科技學系] 期刊論文 2012-09 Placenta proteome analysis from Down syndrome pregnancies for biomarker discovery Chih-Ping Chen; You-Hsuan Chen; Schu-Rern Chern; Shing-Jyh Chang; Te-Lung Tsai; Sheng-Hsiang Li; Hsiu-Chuan Chou; Yi-Wen Lo; Ping-Chiang Lyu; Hong-Lin Chan
    [生物科技學系] 期刊論文 2012-03 Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR and aCGH analyses on uncultured amniocytes for rapid distinguishing true mosaicism from pseudomosaicism Chih-Ping Chen; Hsu-Kuang Huang; Yi-Ning Su; Schu-Rern Chern; Jun-Wei Su; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Yu-Ting Chen; Wayseen Wang
    [生物科技學系] 期刊論文 2010-12 Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Po-Tsang Chen; Wayseen Wang
    [生物科技學系] 期刊論文 2010-06 Fetal cystic lung lesions: Evaluation with magnetic resonance imaging Yu-Peng Liu; Chih-Ping Chen; Shin-Lin Shih; Yi-Fang Chen; Fei-Shih Yang; Su-Chiu Chen
    [生物科技學系] 期刊論文 2010-03 Ventriculomegaly, intrauterine growth restriction and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2->pter) in a fetus Chih-Ping Chen; Yu-Peng Liu; Shaun-Pei Lin; Ming Chen; Fuu-Jen Tsai; Yu-Ting Chen; Li-Feng Chen; Jonathan Kwei Hwang; Wayseen Wang
    [生物科技學系] 期刊論文 2009-12 22q 11.2 Microdeletion in a Fetus With Double-outlet Right Ventricle, Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis by Array Comparative Genomic Hybridization Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Schu-Rern Chern; Fuu-Jen Tsai; Jonathan Kwei Hwang; Wayseen Wang
    [生物科技學系] 期刊論文 2009-09 PRENATAL DIAGNOSIS AND MOLECULAR ANALYSIS OF TRIPLOIDY IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, RELATIVE MACROCEPHALY AND HOLOPROSENCEPHALY Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Kevin Ko; Wayseen Wang
    [生物科技學系] 期刊論文 2009-09 PRENATAL DIAGNOSIS AND MOLECULAR ANALYSIS OF TRISOMY 13 MOSAICISM Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Hung-Hung Lin; Chen-Wen Pan; Wayseen Wang
    [生物科技學系] 期刊論文 2008-03 PRENATAL SONOGRAPHIC AND MAGNETIC RESONANCE IMAGING DEMONSTRATION OF A RIGHT MIDLINE ARACHNOID CYST ASSOCIATED WITH VENTRICULOMEGALY, COLPOCEPHALY, DILATION OF THE THIRD VENTRICLE, ABSENCE OF CAVUM SEPTI PELLUCIDI, AGENESIS OF THE CORPUS CALLOSUM AND MEGA Cisterna Magna Chih-Ping Chen; Tung-Yao Chang; Jeng-Hsiu Hung; Chen-Yu Chen; Wayseen Wang
    [資訊工程學系] 博碩士論文 2008 Designing an Interactive Teaching System by Using Scaffolding Theory -A Case Study of Rei Jhu Elementary School at NanTou County Chih-Ping Chen
    [醫學暨健康學院] 期刊論文 2008-02 XRCC4 Codon 247*A and XRCC4 Promoter-1394*T Related Genotypes but not XRCC4 Intron 3 Gene Polymorphism Are Associated With Higher Susceptibility for Endometriosis Hsieh Yao-Yuan; Da-Tian Bau; Chi-Chen Chang; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai
    [醫學暨健康學院] 期刊論文 2008-01 Association of interleukin-18 gene polymorphism with asthma in Chinese patients Cheng-Chun Lee; Wei-Yong Lin; Lei Wan; Chang-Hai Tsai; Chung-Ming Huang; Chih-Ping Chen; Fuu-Jen Tsai
    [醫學暨健康學院] 期刊論文 2007-12 Growth Hormone (GH) Receptor C.1319 G>T Polymorphism, But Not Exon 3, Retention or Deletion Is Associated With Better First-Year Growth Response to GH Therapy in Patients With GH Deficiency Lei Wan; Chen, WC; Yuhsin Tsai; Kao, YT; Hsieh Yao-Yuan; Cheng-Chun Lee; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai
    [醫學暨健康學院] 期刊論文 2007-09 Human Gene Mutations. Gene symbol: EXT2. Disease: Exostoses (multiple) 2 Wei-De Lin; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback