학술논문


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'학술논문' 에서 검색결과 131건 | 목록 1~20
Academic Journal
Ansari M; South East Scotland Genetic Service, Western General Hospital, Edinburgh, UK.; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK.; Halachev M; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK.; Parry D; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK.; Campos JL; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK.; D'Souza EN; Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.; Barnett C; Faculty of Health and Medical Sciences, University of Adelaide, Adelaide, South Australia, Australia.; Wilkie AOM; MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.; Craniofacial Unit, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.; Barnicoat A; Clinical Genetics, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.; Patel CV; Genetic Health Queensland, Royal Brisbane & Women's Hospital, Brisbane, Queensland, Australia.; Sukarova-Angelovska E; Clinical Genetics, University Pediatric Clinic, Ss. Cyril and Methodius University in Skopje, Skopje, North Macedonia.; Girisha KM; Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India.; Firth HV; Clinical Genetics, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.; Prescott K; Yorkshire Regional Genetics Service, Chapel Allerton Hospital, Leeds, UK.; Wilson LC; Clinical Genetics, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.; McEntagart M; Medical Genetics, St. George's University Hospitals NHS FT, London, UK.; Davidson R; West of Scotland Regional Genetics Service, Queen Elizabeth University Hospital, Glasgow, UK.; Lynch SA; Department of Clinical Genetics, Children's Health Ireland, University College Dublin School of Medicine, Dublin, Ireland.; Joss S; West of Scotland Regional Genetics Service, Queen Elizabeth University Hospital, Glasgow, UK.; Holden ST; Clinical Genetics, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.; Lam WK; South East Scotland Genetic Service, Western General Hospital, Edinburgh, UK.; Sisodiya SM; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.; Chalfont Centre for Epilepsy, Chalfont Saint Peter, UK.; Green AJ; Department of Clinical Genetics, Children's Health Ireland, University College Dublin School of Medicine, Dublin, Ireland.; Poke G; Central Hub, Genetic Health Service, Wellington, New Zealand.; Whiffin N; Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.; FitzPatrick DR; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK.; Meynert A; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK.
Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: eCollection Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Academic Journal
Trajkova S; Department of Neurosciences Rita Levi-Montalcini, University of Turin, Turin 10126, Italy.; Kerkhof J; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A5W9, Canada.; Rossi Sebastiano M; Molecular Biotechnology Center 'Guido Tarone' University of Turin, 10126 Turin, Italy; Department of Molecular Biotechnology and Health Sciences, University of Turin, CASSMedChem, 10126 Turin, Italy.; Pavinato L; Department of Medical Sciences, University of Turin, 10126 Turin, Italy.; Ferrero E; Department of Medical Sciences, University of Turin, 10126 Turin, Italy.; Giovenino C; Department of Medical Sciences, University of Turin, 10126 Turin, Italy.; Carli D; Department of Medical Sciences, University of Turin, 10126 Turin, Italy.; Di Gregorio E; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, 10126 Turin, Italy.; Marinoni R; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, 10126 Turin, Italy.; Mandrile G; Medical Genetics Unit and Thalassemia Center, San Luigi University Hospital, Orbassano, TO 10049, Italy.; Palermo F; Medical Genetics Unit and Thalassemia Center, San Luigi University Hospital, Orbassano, TO 10049, Italy.; Carestiato S; Department of Neurosciences Rita Levi-Montalcini, University of Turin, Turin 10126, Italy.; Cardaropoli S; Department of Public Health and Pediatric Sciences, University of Turin, 10126 Turin, Italy.; Pullano V; Department of Neurosciences Rita Levi-Montalcini, University of Turin, Turin 10126, Italy.; Rinninella A; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, 10126 Turin, Italy; Department of Biomedical and Biotechnological Sciences, Medical Genetics, University of Catania, 94124 Catania, Italy.; Giorgio E; Department of Molecular Medicine, University of Pavia, 27100 Pavia, Italy; Neurogenetics Research Center, IRCCS Mondino Foundation, 27100 Pavia, Italy.; Pippucci T; IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.; Dimartino P; Department of Molecular Medicine, University of Pavia, 27100 Pavia, Italy.; Rzasa J; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A5W9, Canada.; Rooney K; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada.; McConkey H; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada.; Petlichkovski A; Department of Immunology and Human Genetics, Faculty of Medicine, University 'Sv. Kiril I Metodij', Skopje 1000, Republic of Macedonia.; Pasini B; Department of Medical Sciences, University of Turin, 10126 Turin, Italy; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, 10126 Turin, Italy.; Sukarova-Angelovska E; Department of Endocrinology and Genetics, Faculty of Medicine, University 'Sv. Kiril I Metodij', Skopje 1000, Republic of Macedonia.; Campbell CM; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester M13 9WL, UK.; Metcalfe K; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester M13 9WL, UK.; Jenkinson S; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester M13 9WL, UK.; Banka S; Manchester Centre for Genomic Medicine, St. Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester M13 9WL, UK; Division of Evolution, Infection & Genomics, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester M13 9WL, UK.; Mussa A; Department of Public Health and Pediatric Sciences, University of Turin, 10126 Turin, Italy; Pediatric Clinical Genetics Unit, Regina Margherita Childrens' Hospital, 10126 Turin, Italy.; Ferrero GB; Department of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.; Sadikovic B; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada.; Brusco A; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, 10126 Turin, Italy; Department of Neurosciences Rita Levi-Montalcini, University of Turin, Turin 10126, Italy. Electronic address: alfredo.brusco@unito.it.
Publisher: Elsevier Inc Country of Publication: United States NLM ID: 101772885 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2666-2477 (Electronic) Linking ISSN: 26662477 NLM ISO Abbreviation: HGG Adv Subsets: MEDLINE
Academic Journal
Giovenino C; Department of Medical Sciences, University of Turin, 10126, Turin, Italy.; Trajkova S; Department of Medical Sciences, University of Turin, 10126, Turin, Italy.; Pavinato L; Department of Medical Sciences, University of Turin, 10126, Turin, Italy.; Cardaropoli S; Department of Public Health and Pediatrics, University of Turin, 10126, Turin, Italy.; Pullano V; Department of Medical Sciences, University of Turin, 10126, Turin, Italy.; Ferrero E; Department of Medical Sciences, University of Turin, 10126, Turin, Italy.; Sukarova-Angelovska E; Department of Endocrinology and Genetics, University Clinic for Pediatric Diseases, Faculty of Medicine, Ss. Cyril and Methodius University in Skopje, 1000, Skopje, Republic of North Macedonia.; Carestiato S; Department of Medical Sciences, University of Turin, 10126, Turin, Italy.; Salmin P; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, 10126, Turin, Italy.; Rinninella A; Department of Medical Sciences, University of Turin, 10126, Turin, Italy.; Department of Biomedical and Biotechnological Sciences, Medical Genetics, University of Catania, 94124, Catania, Italy.; Battaglia A; Department of Medical Sciences, University of Turin, 10126, Turin, Italy.; Bertoli L; Functional Genomics Lab, Department of Biotechnology, University of Verona, 37134, Verona, Italy.; Fadda A; Functional Genomics Lab, Department of Biotechnology, University of Verona, 37134, Verona, Italy.; Palermo F; Department of Medical Sciences, University of Turin, 10126, Turin, Italy.; Carli D; Department of Public Health and Pediatrics, University of Turin, 10126, Turin, Italy.; Mussa A; Department of Public Health and Pediatrics, University of Turin, 10126, Turin, Italy.; Dimartino P; Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.; Bruselles A; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146, Rome, Italy.; Froukh T; Department of Biotechnology and Genetic Engineering, Philadelphia University, Amman, Jordan.; Mandrile G; Medical Genetics Unit and Thalassemia Center, San Luigi University Hospital, University of Torino, Orbassano, TO, Italy.; Pasini B; Department of Medical Sciences, University of Turin, 10126, Turin, Italy.; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, 10126, Turin, Italy.; De Rubeis S; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.; Buxbaum JD; Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.; The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.; Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.; Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.; Pippucci T; U.O. Genetica Medica, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italia.; Tartaglia M; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146, Rome, Italy.; Rossato M; Functional Genomics Lab, Department of Biotechnology, University of Verona, 37134, Verona, Italy.; Delledonne M; Functional Genomics Lab, Department of Biotechnology, University of Verona, 37134, Verona, Italy.; Ferrero GB; Department of Public Health and Pediatrics, University of Turin, 10126, Turin, Italy.; Brusco A; Department of Medical Sciences, University of Turin, 10126, Turin, Italy. alfredo.brusco@unito.it.; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, 10126, Turin, Italy. alfredo.brusco@unito.it.
Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE
Academic Journal
Bratislavske lekarske listy. 108(8)
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[검색어] Sukarova-Angelovska, E.
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