학술논문
전자자료 공정이용 안내
우리 대학 도서관에서 구독·제공하는 모든 전자자료(데이터베이스, 전자저널, 전자책 등)는 국내외 저작권법과 출판사와의 라이선스 계약에 따라 엄격하게 보호를 받고 있습니다.
전자자료의 비정상적 이용은 출판사로부터의 경고, 서비스 차단, 손해배상 청구 등 학교 전체에 심각한 불이익을 초래할 수 있으므로, 아래의 공정이용 지침을 반드시 준수해 주시기 바랍니다.
공정이용 지침
- 전자자료는 개인의 학습·교육·연구 목적의 비영리적 사용에 한하여 이용할 수 있습니다.
- 합리적인 수준의 다운로드 및 출력만 허용됩니다. (일반적으로 동일 PC에서 동일 출판사의 논문을 1일 30건 이하 다운로드할 것을 권장하며, 출판사별 기준에 따라 다를 수 있습니다.)
- 출판사에서 제공한 논문의 URL을 수업 관련 웹사이트에 게재할 수 있으나, 출판사 원문 파일 자체를 복제·배포해서는 안 됩니다.
- 본인의 ID/PW를 타인에게 제공하지 말고, 도용되지 않도록 철저히 관리해 주시기 바랍니다.
불공정 이용 사례
- 전자적·기계적 수단(다운로딩 프로그램, 웹 크롤러, 로봇, 매크로, RPA 등)을 이용한 대량 다운로드
- 동일 컴퓨터 또는 동일 IP에서 단시간 내 다수의 원문을 집중적으로 다운로드하거나, 전권(whole issue) 다운로드
- 저장·출력한 자료를 타인에게 배포하거나 개인 블로그·웹하드 등에 업로드
- 상업적·영리적 목적으로 자료를 전송·복제·활용
- ID/PW를 타인에게 양도하거나 타인 계정을 도용하여 이용
- EndNote, Mendeley 등 서지관리 프로그램의 Find Full Text 기능을 이용한 대량 다운로드
- 출판사 콘텐츠를 생성형 AI 시스템에서 활용하는 행위(업로드, 개발, 학습, 프로그래밍, 개선 또는 강화 등)
위반 시 제재
- 출판사에 의한 해당 IP 또는 기관 전체 접속 차단
- 출판사 배상 요구 시 위반자 개인이 배상 책임 부담
'학술논문'
에서 검색결과 1,076건 | 목록
1~20
Academic Journal
Compàs d'amalgama; No 10 (2024): Compas d'amalgama; 28-35
Compàs d'amalgama; No. 10 (2024): Compas d'amalgama; 28-35
Compàs d'amalgama; Núm. 10 (2024): Compas d'amalgama; 28-35
Compas d'amalgama; N. 10 (2024): Compas d'amalgama; 28-35
RCUB. Revistas Científicas de la Universidad de Barcelona
instname
Compàs d'amalgama; No. 10 (2024): Compas d'amalgama; 28-35
Compàs d'amalgama; Núm. 10 (2024): Compas d'amalgama; 28-35
Compas d'amalgama; N. 10 (2024): Compas d'amalgama; 28-35
RCUB. Revistas Científicas de la Universidad de Barcelona
instname
Academic Journal
Journal of Catalan Intellectual History = Revista d'història de la filosofia catalana; 4 : issue 7/8 (2014); p. 171-173
Academic Journal
Schmetz, A.; Lüdecke, H. J.; Surowy, H.; Sivalingam, S.; Bruel, A. L.; Caumes, R.; Charles, P.; Chatron, N.; Chrzanowska, K.; Codina-Solà, M.; Colson, C.; Cuscó, I.; Denommé-Pichon, A. S.; Edery, P.; Faivre, L.; Green, A.; Heide, S.; Hsieh, T. C.; Hustinx, A.; Kleinendorst, L.; Knopp, C.; Kraft, F.; Krawitz, P. M.; Lasa-Aranzasti, A.; Lesca, G.; López-González, V.; Maraval, J.; Mignot, C.; Neuhann, T.; Netzer, C.; Oehl-Jaschkowitz, B.; Petit, Florence; Philippe, C.; Posmyk, R.; Putoux, A.; Reis, A.; Sánchez-Soler, M. J.; Suh, J.; Tkemaladze, T.; Tran Mau Them, F.; Travessa, A.; Trujillano, L.; Valenzuela, I.; van Haelst, M. M.; Vasileiou, G.; Vincent-Delorme, C.; Walther, M.; Verde, P.; Bramswig, N. C.; Wieczorek, D.
Schmetz, A, Lüdecke, H-J, Surowy, H, Sivalingam, S, Bruel, A-L, Caumes, R, Charles, P, Chatron, N, Chrzanowska, K, Codina-Solà, M, Colson, C, Cuscó , I , Denommé-Pichon, A-S, Edery, P, Faivre, L, Green, A, Heide, S, Hsieh, T-C, Hustinx, A, Kleinendorst, L, Knopp, C, Kraft, F, Krawitz, P M, Lasa-Aranzasti, A, Lesca, G, López-González, V, Maraval, J, Mignot, C, Neuhann, T, Netzer, C, Oehl-Jaschkowitz, B, Petit, F, Philippe, C, Posmyk, R, Putoux, A, Reis, A, Sánchez-Soler, M J, Suh, J, Tkemaladze, T, Tran Mau Them, F, Travessa, A, Trujillano, L, Valenzuela, I , van Haelst, M M, Vasileiou, G, Vincent-Delorme, C, Walther, M, Verde, P, Bramswig, N C & Wieczorek, D 2023, 'Delineation of the adult phenotype of Coffin–Siris syndrome in 35 individuals', Human Genetics. https://doi.org/10.1007/s00439-023-02622-5
Academic Journal
ANDORRA I LA MULTICULTURALITAT 33A DIADA ANDORRANA A L’UCE: 11-15 (2021). (33)
Academic Journal
Articles publicats en revistes (Història de l'Art)
Dipòsit Digital de la UB
instname
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
Dipòsit Digital de la UB
instname
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
Academic Journal
Trujillano L; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Valenzuela I; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Costa-Roger M; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Cuscó I; Genetics Department, Institut d'Investigació Biomèdica Sant Pau (IIB SANT PAU), Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.; Fernandez-Alvarez P; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Cueto-González A; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Lasa-Aranzasti A; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Masotto B; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Abulí A; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Codina-Solà M; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Del Campo M; Department of Clinical Pediatrics, University of California, San Diego, California, USA.; Ruiz Moreno JA; Department of Pediatrics, Hospital Costa del Sol, Marbella, Málaga, Spain.; Pardo Domínguez C; Department of Pediatrics, Hospital Costa del Sol, Marbella, Málaga, Spain.; Palma Milla C; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; UDISGEN (Unidad de Dismorfología y Genética), Hospital Universitario 12 de Octubre, Madrid, Spain.; Pérez de la Fuente R; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; UDISGEN (Unidad de Dismorfología y Genética), Hospital Universitario 12 de Octubre, Madrid, Spain.; Quesada-Espinosa JF; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; UDISGEN (Unidad de Dismorfología y Genética), Hospital Universitario 12 de Octubre, Madrid, Spain.; Núñez-Enamorado N; Departamento de Neurología pediátrica, Hospital Universitario 12 de Octubre, Madrid, Spain.; Gener B; Department of Genetics, Cruces University Hospital, Biobizkaia Health Research Institute, Vizcaya, Spain.; Ballesta-Martínez MJ; Sección Genética Médica, Servicio de Pediatría, Hospital Clinico Universitario Virgen de la Arrixaca, Murcia, Spain.; Brea-Fernández AJ; Grupo de Genómica y Bioinformática, Centro Singular de Investigación en Medicina Molecular y Enfermedades Crónicas (CiMUS), Centro de Investigación Biomédica en Red de Enfermedades Raras del Instituto de Salud Carlos III (CIBERER-ISCIII), Universidade de Santiago de Compostela, Santiago de Compostela, Spain.; Fundación Pública Galega Instituto de Investigación Sanitaria de Santiago de Compostela (FIDIS), Santiago de Compostela, Spain.; Fernández-Prieto M; Grupo de Genómica y Bioinformática, Centro Singular de Investigación en Medicina Molecular y Enfermedades Crónicas (CiMUS), Centro de Investigación Biomédica en Red de Enfermedades Raras del Instituto de Salud Carlos III (CIBERER-ISCIII), Universidade de Santiago de Compostela, Santiago de Compostela, Spain.; Fundación Pública Galega Instituto de Investigación Sanitaria de Santiago de Compostela (FIDIS), Santiago de Compostela, Spain.; Trujillo-Quintero JP; Center for Genomic Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.; Ruiz A; Center for Genomic Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.; Santos-Simarro F; Unidad de Diagnóstico Molecular y Genética Clínica, Hospital Universitario Son Espases, Idisba, Palma de Mallorca, Spain.; Rosello M; Genetics Unit, Hospital Universitario y Politecnico La Fe, Valencia, Spain.; Orellana C; Genetics Unit, Hospital Universitario y Politecnico La Fe, Valencia, Spain.; Martinez F; Genetics Unit, Hospital Universitario y Politecnico La Fe, Valencia, Spain.; Martinez-Monseny AF; Department of Genetics and Institut de Recerca, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.; Casas-Alba D; Department of Genetics and Institut de Recerca, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.; Serrano M; Pediatric Neurology Department, Institut de Recerca, Hospital Sant Joan de Déu, Barcelona, Spain.; Palomares-Bralo M; Clinical Genetics Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, CIBERER, Hospital Universitario La Paz, Madrid, Spain.; Rikeros-Orozco E; Clinical Genetics Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, CIBERER, Hospital Universitario La Paz, Madrid, Spain.; Gómez-Cano MÁ; Clinical Genetics Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, CIBERER, Hospital Universitario La Paz, Madrid, Spain.; Tirado-Requero P; Neuropediatric Unit, University Hospital La Paz, Madrid, Spain.; Pié Juste J; Unit of Clinical Genetics and Functional Genomics, Department of Pharmacology-Physiology, School of Medicine, Universidad de Zaragoza, CIBERER-GCV02 and IIS-Aragon, Zaragoza, Spain.; Ramos FJ; Unit of Clinical Genetics and Functional Genomics, Department of Pharmacology-Physiology, School of Medicine, Universidad de Zaragoza, CIBERER-GCV02 and IIS-Aragon, Zaragoza, Spain.; Unit of Clinical Genetics, Service of Paediatrics, University Hospital 'Lozano Blesa', University of Zaragoza Medical School, CIBERER-GCV02 and IIS-Aragon, Zaragoza, Spain.; García-Arumí E; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Tizzano EF; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.
Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
검색 결과 제한하기
제한된 항목
[검색어] Cuscó, I
발행연도 제한
-
학술DB(Database Provider)
저널명(출판물, Title)
출판사(Publisher)
자료유형(Source Type)
주제어
언어