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우리 대학 도서관에서 구독·제공하는 모든 전자자료(데이터베이스, 전자저널, 전자책 등)는 국내외 저작권법과 출판사와의 라이선스 계약에 따라 엄격하게 보호를 받고 있습니다.
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'e-Article' searched 105results | List 1~20
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Academic Journal
Coudert A; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Le Tanno P; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Dufour W; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Edery P; Hospices Civils de Lyon, Lyon, France.; Jacquette A; Service de génétique, CHICAM Site Alençon, Alençon, France.; Delplancq G; Unité de génétique constitutionnelle, service de biologie médicale, CH Versailles, Le Chesnay, France.; Chambon P; Laboratoire de Cytogénétique, CHU Rouen, Rouen, France.; Missirian C; Département de Génétique médicale, Hôpital de la Timone-Enfant, Assistance Publique Hôpitaux de Marseille, Hopital de la Timone, Marseille, France.; Caumes R; Service de génétique clinique, CHU Lille, Lille, France.; Faivre L; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, CHU Dijon, Dijon, France.; Callier P; Laboratoire de génétique chromosomique et moléculaire, CHU Dijon, Dijon, France.; Mosca AL; Laboratoire de génétique chromosomique et moléculaire, CHU Dijon, Dijon, France.; Marle N; Laboratoire de génétique chromosomique et moléculaire, CHU Dijon, Dijon, France.; Geneviève D; Université Montpellier, U1183, Service de Génétique Médicale, CHU Montpellier, Montpellier, France.; Lacombe D; Service de Génétique Médicale et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, CHU Bordeaux; INSERM U1211, Bordeaux, France.; Pebrel-Richard C; Service de Cytogénétique - Secteur constitutionnel, CHU Clermont-Ferrand, Clermont-Ferrand, France.; Redon S; Service de Génétique Médicale et Biologie de la Reproduction, CHU de Brest, Brest, France and Univ Brest, Inserm, EFS, UMR 1078, GGB, F-29200, Brest, France.; Touraine R; Service de génétique clinique chromosomique et moléculaire, CHU Saint-Etienne, Saint Etienne, France.; Fradin M; Service de génétique clinique, centre de référence maladies rares anomalies du développement CLAD-Ouest, CHU, Rennes, France.; Odent S; Service de génétique clinique, centre de référence maladies rares anomalies du développement CLAD-Ouest, CHU, Rennes, France.; Pasquier L; Service de génétique clinique, centre de référence maladies rares anomalies du développement CLAD-Ouest, CHU, Rennes, France.; Guichet A; Department of Genetics, University Hospital of Angers, Angers, France.; Mercier S; Université de Rennes 1, UEB, IFR 140, Faculté de Médecine, CNRS, UMR 6061, Institut Génétique et Développement de Rennes, Rennes, France.; Medical Genetics, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Nizon M; Medical Genetics, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Isidor B; Medical Genetics, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Vincent M; Medical Genetics, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Le Guillou Horn XM; LabCom I3M-Dactim mis/LMA CNRS 7348, Université de Poitiers, Poitiers, France.; Egloff M; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Schaefer E; Hôpitaux Universitaires de Strasbourg, Service de Génétique Médicale, Strasbourg, France.; Guerrot AM; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Ruaud L; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Chemaly N; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Nadeau G; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Coutton C; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France.; Dieterich K; Univ. Grenoble Alpes, Inserm U1209, IAB, CHU Grenoble Alpes, Grenoble, France KDieterich@chu-grenoble.fr.
Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Academic Journal
Cetica, V, Pisano, T, Lesca, G, Marafi, D, Licchetta, L, Riccardi, F, Mei, D, Chung, H Y B, Bayat, A, Balasubramanian, M, Lowenstein, D H, Endzinienė, M, Alotaibi, M, Villeneuve, N, Jacobs, J, Isidor, B, Solazzi, R, den Hollander, N S, Marjanovic, D, Rougeot-Jung, C, Jung, J, Lesieur-Sebellin, M, Accogli, A, Salpietro, V, Saadi, N W, Panagiotakaki, E, Foiadelli, T, Redon, S, Tsai, M H, Bisulli, F, Hammer, T B, Lupski, J R, Parrini, E & Guerrini, R 2024, ' Clinical and molecular characterization of patients with YWHAG-related epilepsy ', Epilepsia, vol. 65, no. 5, pp. 1439-1450 . https://doi.org/10.1111/epi.17939
Academic Journal
Furia F; Department of Epilepsy Genetics and Personalized Treatment, The Danish Epilepsy Centre, Dianalund, Denmark.; Faculty of Health Science, University of Southern Denmark (SDU), Odense, Denmark.; Levy AM; Department of Clinical Genetics, Kennedy Center, Copenhagen University Hospital, Copenhagen, Denmark.; Theunis M; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.; Bamshad MJ; Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, Washington, USA.; Brotman-Baty Institute for Precision Medicine, University of Washington, Seattle, Washington, USA.; Department of Pediatrics, Division of Genetic Medicine, Seattle Children's Hospital, Seattle, Washington, USA.; Bartos MN; Department of Genetics, The University of Alabama at Birmingham, Birmingham, Alabama, USA.; Bijlsma EK; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.; Brancati F; Human Genetics, Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.; Human Functional Genetics Laboratory, Istituto di Ricovero e Cura a Carattere Scientifico San Raffaele Roma, Rome, Italy.; Cejudo L; CHU de Poitiers, Service de Génétique, Poitiers, France.; Chong JX; Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, Washington, USA.; Brotman-Baty Institute for Precision Medicine, University of Washington, Seattle, Washington, USA.; De Luca C; Human Genetics, Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.; Dean SJ; Department of Genetics, The University of Alabama at Birmingham, Birmingham, Alabama, USA.; Egense A; Division of Genomic Medicine, Department of Pediatrics, University of California Davis, Sacramento, California, USA.; Goel H; General Genetics Service, Hunter Genetics, Waratah, New South Wales, Australia.; School of Medicine and Public Health, College of Health, Medicine and Wellbeing, University of Newcastle, Callaghan, New South Wales, Australia.; Guenzel AJ; GeneDx Inc., Gaithersburg, Maryland, USA.; Hüffmeier U; Institute of Human Genetics, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.; Legius E; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.; Mancini GMS; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.; ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus MC University Medical Center, Rotterdam, The Netherlands.; Marcos-Alcalde I; Molecular Modeling Group, Centro de Biología Molecular Severo Ochoa (CBM, CSIC-UAM), Madrid, Spain.; Niclass T; CHU de Poitiers, Service de Génétique, Poitiers, France.; Planes M; Service de Génétique Clinique, CHRU de Brest, Brest, France.; Redon S; Service de Génétique Médicale et Biologie de la Reproduction, CHU de Brest, Brest, France.; Université de Brest, INSERM, Etablissement Français du Sang, UMR 1078, Brest, France.; Ros-Pardo D; Molecular Modeling Group, Centro de Biología Molecular Severo Ochoa (CBM, CSIC-UAM), Madrid, Spain.; Rouault K; Service de Génétique Médicale et Biologie de la Reproduction, CHU de Brest, Brest, France.; Université de Brest, INSERM, Etablissement Français du Sang, UMR 1078, Brest, France.; Schot R; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.; Discovery Unit, Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.; Schuhmann S; Institute of Human Genetics, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.; Shen JJ; Division of Genomic Medicine, Department of Pediatrics, University of California Davis, Sacramento, California, USA.; Tao AM; Vagelos School of Physicians and Surgeons, Columbia University, New York, New York, USA.; Thiffault I; Department of Pathology, Children's Mercy Kansas City, Kansas City, Missouri, USA.; Genomic Medicine Center, Children's Mercy Kansas City, Kansas City, Missouri, USA.; Van Esch H; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.; Laboratory for the Genetics of Cognition, KU Leuven, Leuven, Belgium.; Wentzensen IM; GeneDx Inc., Gaithersburg, Maryland, USA.; Barakat TS; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.; ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus MC University Medical Center, Rotterdam, The Netherlands.; Discovery Unit, Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.; Møller RS; Department of Epilepsy Genetics and Personalized Treatment, The Danish Epilepsy Centre, Dianalund, Denmark.; Faculty of Health Science, University of Southern Denmark (SDU), Odense, Denmark.; Gomez-Puertas P; Molecular Modeling Group, Centro de Biología Molecular Severo Ochoa (CBM, CSIC-UAM), Madrid, Spain.; Chung WK; Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA.; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.; Gardella E; Department of Epilepsy Genetics and Personalized Treatment, The Danish Epilepsy Centre, Dianalund, Denmark.; Faculty of Health Science, University of Southern Denmark (SDU), Odense, Denmark.; Department of Neurophysiology, The Danish Epilepsy Centre, Dianalund, Denmark.; Tümer Z; Department of Clinical Genetics, Kennedy Center, Copenhagen University Hospital, Copenhagen, Denmark.; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
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
Academic Journal
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BRAIN; MAY 3 2024, 147 5, p1837-p1855, 19p.
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자료유형(Source Type)
Subject
Language