학술논문


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'학술논문' 에서 검색결과 377건 | 목록 1~20
Academic Journal
Nava, CarolineCogne, BenjaminSantini, AmandineLeitão, ElsaLecoquierre, FrançoisChen, YuyangStenton, Sarah L.Besnard, ThomasHeide, SolveigBaer, SarahJakhar, AbhilashaNeuser, SonjaKeren, BorisFaudet, AnneForlani, SylvieFaoucher, MarieUguen, KevinPlatzer, KonradAfenjar, AlexandraAlessandri, Jean-LucAndres, StephanieAngelini, ChloéAral, BernardArveiler, BenoitAttie-Bitach, TaniaAubert Mucca, MarionBanneau, GuillaumeBarakat, Tahsin StefanBarcia, GiuliaBaulac, StéphanieBeneteau, ClaireBenkerdou, FouziaBernard, VirginieBézieau, StéphaneBonneau, DominiqueBonnet-Dupeyron, Marie-NoelleBoussion, SimonBoute, OdileBrischoux-Boucher, EliseBryen, Samantha J.Buratti, JulienBusa, TiffanyCaliebe, AlmuthCapri, YlineCassinari, KévinCaumes, RoselineCenni, CamilleChambon, PascalCharles, PerrineChristodoulou, JohnColson, CindyConrad, SolèneCospain, AurianeCoursimault, JulietteCourtin, ThomasCouse, MadelineCoutton, CharlesCreveaux, IsabelleD’Gama, Alissa M.Dauriat, Benjaminde Sainte Agathe, Jean-MadeleineDel Gobbo, GiuliaDelahaye-Duriez, AndréeDelanne, JulianDenommé-Pichon, Anne-SophieDieux-Coeslier, AnneDo Souto Ferreira, LauraDoco-Fenzy, MartineDrukewitz, StephanDuboc, VéroniqueDubourg, ChristèleDuffourd, YannisDyment, DavidEl Chehadeh, SalimaElmaleh, MoniqueFaivre, LaurenceFennelly, SamuelFischer, HannaFradin, MélanieGalludec Vaillant, CamilleGanne, BenjaminGhoumid, JamalGoel, HimanshuGokce-Samar, ZeynepGoldenberg, AliceGonfreville Robert, RomainGorokhova, SvetlanaGoujon, LouiseGranier, VictoriaGras, MathildeGreally, John M.Greiten, BiancaGueguen, PaulGuerrot, Anne-MarieGuha, SauravGuimier, AnneHaack, Tobias B.Hadj Abdallah, HamzaHalleb, YosraHarbuz, RaduHarris, MadeleineHentschel, JuliaHéron, BénédicteHitz, Marc-PhillipInnes, A. MicheilJadas, VincentJanuel, LouisJean-Marçais, NolwennJobanputra, VaidehiJobic, FlorenceJornea, LudmilaJost, CélineJulia, SophieKaiser, Frank J.Kaschta, DanielKaya, SabineKetteler, PetraKhadija, BochraKilpert, FabianKnopp, CordulaKraft, FlorianKrey, IlonaLackmy, MarilynLaffargue, FannyLambert, LaetitiaLamont, RyanLaugel, VincentLaurie, StevenLauzon, Julie L.Lebreton, LouisLebrun, MarineLegendre, MarineLeguern, EricLehalle, DaphnéLejeune, ElodieLesca, GaetanLesieur-Sebellin, MarionLevy, JonathanLinglart, AgnèsLyonnet, StanislasLüthy, KevinMa, Alan S.Mach, CorinneMandel, Jean-LouisMansour-Hendili, LamisseMarcadier, JulienMarin, VictorMargot, HenriMarquet, ValentineMay, AngèleMayr, Johannes A.Meridda, CatherineMichaud, VincentMichot, CarolineNadeau, GwenaelNaudion, SophieNguyen, LaetitiaNizon, MathildeNowak, FrédériqueOdent, SylvieOlin, ValerieOsei-Owusu, Ikeoluwa A.Osmond, MatthewÕunap, KatrinPasquier, LaurentPassemard, SandrinePauly, MelissaPatat, OlivierPensec, MarinePerrin-Sabourin, LaurencePetit, FlorencePhilippe, ChristophePlanes, MarcPoduri, AnnapurnaPoirsier, CélinePouzet, AntoinePrince, BradleyProuteau, ClémentPujol, AuroraRacine, CarolineRama, MélanieRamond, FrancisRanguin, KaraRaway, MargauxReis, AndréRenaud, MathildeRevencu, NicoleRichard, Anne-ClaireRiera-Navarro, LucileRius, RocioRodriguez, DianaRodriguez-Palmero, AgustíRondeau, SophieRoser-Unruh, AnnikaRougeot Jung, ChristelleSafraou, HanaSatre, VéroniqueSaugier-Veber, PascaleSauvestre, ClémentSchaefer, EliseShao, WanqingSchanze, InaSchlump, Jan-UlrichSchlüter Martin, AgathaSchluth-Bolard, CarolineSchuhmann, SarahSchröder, ChristopherSebastin, MonishaSigaudy, SabineSpielmann, MalteSpodenkiewicz, MartaSt Clair, LauraSteffann, JulieStoeva, RadkaSurowy, HaraldTarnopolsky, Mark A.Todosi, CalinaToutain, AnnickTran Mau-Them, FrédéricUnterlauft, AstridVan-Gils, JulienVanlerberghe, ClémenceVasileiou, GeorgiaVera, GabriellaVerdel, AndréVerloes, AlainVial, YoannVignal, CédricVincent, MarieVincent-Delorme, CatherineVincent-Devulder, AlineVitobello, AntonioWeber, SachaWillems, MarjolaineZaafrane-Khachnaoui, KhaoulaZacher, PiaZeltner, LenaZiegler, AlbanGalej, Wojciech P.Dollfus, HélèneThauvin, ChristelBoycott, Kym M.Marijon, PierreLermine, AlbanMalan, ValérieRio, MarlèneKuechler, AlmaIsidor, BertrandDrunat, SéverineSmol, ThomasChatron, NicolasPiton, AmélieNicolas, GaelWagner, MatiasAbou Jamra, RamiHéron, DelphineMignot, CyrilBlanc, PierreO’Donnell-Luria, AnneWhiffin, NicolaCharbonnier, CamilleCharenton, ClémentThevenon, JulienDepienne, Christel
Nature Genetics. :1-15
Academic Journal
Системи управління, навігації та зв’язку. Збірник наукових праць. 4:102-108
Academic Journal
Jedraszak G; Constitutional Genetics Laboratory, University Hospital of Amiens, Amiens, France.; UR4666, University of Picardy Jules Verne, Amiens, France.; Jobic F; Clinical Genetics Unit, University Hospital of Amiens, Amiens, France.; Receveur A; Constitutional Genetics Laboratory, University Hospital of Amiens, Amiens, France.; Bilan F; Genetics Laboratory, University Hospital of Poitiers, Poitiers, France.; Gilbert-Dussardier B; Medical Genetics Unit, University Hospital of Poitiers, Poitiers, France.; Tiffany B; Medical Genetics Unit, University Hospital of Marseille, Marseille, France.; Missirian C; Cytogenetics Laboratory, University Hospital of Marseille, Marseille, France.; Willems M; Medical Genetics Laboratory, University Hospital of Montpellier, Montpellier, France.; Odent S; Medical Genetics Unit, University Hospital of Rennes, Rennes, France.; Lucas J; Genetics Laboratory, University Hospital of Rennes, Rennes, France.; Dubourg C; Molecular & Genomic Institute, Rennes, France.; Schaefer E; Clinical Genetics Unit, University Hospital of Strasbourg, Strasbourg, France.; Scheidecker S; Medical Genetics Laboratory & INSERM U1112, Strasbourg, France.; Lespinasse J; Clinical Genetics Unit, Hospital of Chambéry, Chambéry, France.; Goldenberg A; Clinical Genetics Unit, University Hospital of Rouen, Rouen, France.; Guerrot AM; Clinical Genetics Unit, University Hospital of Rouen, Rouen, France.; Joly-Helas G; Cytogenetics Laboratory, University Hospital of Rouen, Rouen, France.; Chambon P; Cytogenetics Laboratory, University Hospital of Rouen, Rouen, France.; Le Caignec C; Medical Gentics Unit, University Hospital of Toulouse, Toulouse, France.; David A; Clinical Genetics Unit, University Hospital of Nantes, Nantes, France.; Coutton C; Cytogenetics Laboratory, University Hospital of Grenoble & INSERM U1209 Institute for Advanced Biosciences, University of Grenoble Alpes, Grenoble, France.; Satre V; Cytogenetics Laboratory, University Hospital of Grenoble & INSERM U1209 Institute for Advanced Biosciences, University of Grenoble Alpes, Grenoble, France.; Vieville G; Cytogenetics Laboratory, University Hospital of Grenoble, Grenoble, France.; Amblard F; Cytogenetics Laboratory, University Hospital of Grenoble, Grenoble, France.; Harbuz R; Cytogenetics Laboratory, University Hospital of Grenoble, Grenoble, France.; Sanlaville D; Cytogenetics Laboratory, University Hospital of Lyon, Bron, France.; Till M; Cytogenetics Laboratory, University Hospital of Lyon, Bron, France.; Vincent-Delorme C; Catherine Vincent Delorme, Clinical Genetics Unit Guy Fontaine, University Hospital of Lille, Lille, France.; Colson C; Catherine Vincent Delorme, Clinical Genetics Unit Guy Fontaine, University Hospital of Lille, Lille, France.; Andrieux J; Molecular Genetics Institute, University hospital of Lille, Lille, France.; Naudion S; Clinical Genetics Unit, University Hospital of Bordeaux, Bordeaux, France.; Toutain J; Clinical Genetics Unit, University Hospital of Bordeaux, Bordeaux, France.; Rooryck C; Medical Genetics Laboratory, University Hospital of Bordeaux, Bordeaux, France.; de Fréminville B; Genetics Laboratory, University Hospital of Saint-Etienne, Saint-Etienne, France.; Prieur F; Medical Genetics Unit, University Hospital of Saint-Etienne, Saint Etienne, France.; Daire VC; Medical Genetics Federation, Necker-Children's Hospital, Paris, France.; Amram D; Clinicial Genetics Unit, University Hospital of Creteil, Creteil, France.; Kleinfinger P; Cerba Laboratory, Saint-Ouen, France.; Raabe-Meyer G; Praxis für Humangenetik Dr. Schulze, Hannover, Germany.; Courage C; Folkhälsan Research Center, Helsinki, Finland.; Lemke J; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Stefanou EG; Cytogenetics Unit, Laboratory of Medical Genetics, University General Hospital of Patras, Patras, Greece.; Loretta T; Developmental Assessment Unit, National and Kapodistrian University of Athens, Athens, Greece.; Emmanouil M; ATG Genetic Center, Athens, Greece.; Tzeli SK; Department of Medical Genetics, National and Kapodistrian University of Athens, Athens, Greece.; Sodowska H; Niepubliczny Zakład Opieki Zdrowotne 'Genom', Ruda Slaska, Poland.; Anderson J; Cytogenetics Department, Sullivan and Nicolaides Pathology, Taringa, Queensland, Australia.; Nandini A; Department of Cytogenetics, Royal Brisbane and Women's Hospital, Brisbane, Australia.; Copin H; Constitutional Genetics Laboratory, University Hospital of Amiens, Amiens, France.; Garçon L; Constitutional Genetics Laboratory, University Hospital of Amiens, Amiens, France.; UR4666, University of Picardy Jules Verne, Amiens, France.; Liehr T; Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Jena, Germany.; Morin G; Clinical Genetics Unit, University Hospital of Amiens, Amiens, France.
Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Academic Journal
De Jonghe J; The Genome Function Laboratory, The Francis Crick Institute, London, UK.; Kim HC; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK.; Adedeji A; The Genome Function Laboratory, The Francis Crick Institute, London, UK.; Department of Biochemical Engineering, University College London, London, UK.; Leitão E; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Dawes R; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK.; Chen Y; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK.; Blakes AJ; Manchester Centre for Genomic Medicine, Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Simons C; Centre for Population Genomics, Garvan Institute of Medical Research, Sydney, Australia.; Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Australia.; Rius R; Centre for Population Genomics, Garvan Institute of Medical Research, Sydney, Australia.; Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Australia.; Alvi JR; Department of Pediatric Neurology, University of Child Health Sciences, The Children's Hospital, Lahore, Pakistan.; Amblard F; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France.; Austin-Tse C; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Baer S; Service de pédiatrie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Balton EV; Department of Medicine, University of Washington School of Medicine, Seattle, WA, United States.; Blanc P; Laboratoire SeqOIA, Paris, France.; Calame DG; Section of Pediatric Neurology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, TX, USA.; Coutton C; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France.; Cunningham CA; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.; Dargie N; Department of Medicine, University of Washington School of Medicine, Seattle, WA, United States.; Dipple KM; Department of Pediatrics, University of Washington, Seattle, WA, United States.; Brotman Baty Institute for Precision Medicine, Seattle, WA, United States.; Du H; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; El Chehadeh S; Service de Génétique Médicale, Institut de Génétique Médicale D'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Laboratoire de Génétique Médicale, Institut de Génétique Médicale d'Alsace, INSERM UMRS_1112, CRBS, Université de Strasbourg, Strasbourg, France.; Glass I; Department of Pediatrics, University of Washington, Seattle, WA, United States.; Brotman Baty Institute for Precision Medicine, Seattle, WA, United States.; Gleeson JG; Rady Children's Institute for Genomic Medicine, San Diego, CA, USA.; Department of Neurosciences and Pediatrics, University of California, San Diego, San Diego, CA, USA.; Grunewald O; Laboratoire SeqOIA, Paris, France.; U1172-LilNCog-Lille Neuroscience & Cognition, CHU de Lille, Lille, France.; Laboratoire de Genopathies, CHU Lille, Lille, France.; Gueguen P; Laboratoire SeqOIA, Paris, France.; Service de Génétique, CHRU de Tours, Tours, France.; Université de Tours, Imaging Brain & Neuropsychiatry iBraiN U1253, Tours, France.; Harbuz R; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; Jacquemont ML; Service de Génétique, CHRU de Tours, Tours, France.; Université de Tours, Imaging Brain & Neuropsychiatry iBraiN U1253, Tours, France.; Centre de Référence Maladies Rares 'Anomalies du Développement et Syndromes Malformatifs', FHU Genomeds, CHRU de Tours, Tours, France.; Leventer RJ; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.; Royal Children's Hospital, Melbourne, VIC, Australia.; Marijon P; Laboratoire SeqOIA, Paris, France.; Messaoud O; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Harvard Medical School, Boston, MA.; Sultan T; Department of Pediatric Neurology, University of Child Health Sciences, The Children's Hospital, Lahore, Pakistan.; Thauvin C; Centre de référence maladies rares, Déficiences Intellectuelles de Causes Rares, Centre de Génétique, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, Fédération Hospitalo-Universitaire-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; UMR1231 GAD, Inserm, Université Bourgogne-Franche Comté, Dijon, France.; Vincent-Delorme C; Clinique de Génétique, Hôpital Jeanne de Flandre, CHU de Lille, Lille, France.; Consultation de génétique, CH Arras, Arras, France.; Gulec EY; Department of Medical Genetics, Istanbul Medeniyet University Medical School, Istanbul, Turkiye.; Medical Genetics Clinic, Istanbul Goztepe Prof Dr Suleyman Yalcin City Hospital, Istanbul, Turkiye.; Thevenon J; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France.; Mendez R; Cardiovascular Medicine, Stanford University, Stanford, CA, USA.; MacArthur DG; Centre for Population Genomics, Garvan Institute of Medical Research, Sydney, Australia.; Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Australia.; Depienne C; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Nava C; Laboratoire SeqOIA, Paris, France.; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Département de Génétique, Hôpital de la Pitié Salpêtrière, Paris, France.; Whiffin N; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK.; Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Findlay GM; The Genome Function Laboratory, The Francis Crick Institute, London, UK.
Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE
Academic Journal
Вісник Харківського національногоуніверситету імені В.Н. Каразіна. Серія: Радіофізика та електроніка, Iss 27 (2018)
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[검색어] Harbuz, S.
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