부산대학교 도서관

Hallenkamp-Lumpe, J.; Spiong, S.

Archäologie in Deutschland, 2018 Oct 01(5), 60-61.

Oriens Extremus, 1968 Jan 01. 15(1), 83-100.

Macfarlane, GJ; Kronisch, C; Dean, LE; Atzeni, F; Hauser, W; Fluss, E; Choy, E; Kosek, E; Amris, K; Branco, J; Dincer, F; Leino-Arjas, P; Longley, K; McCarthy, GM; Makri, S; Perrot, S; Sarzi-Puttini, P; Taylor, A; Jones, GT

Annals of the rheumatic diseases. 76(2):318-328

Costa, João Pedro; Andrade, Maria J.; Dal Cin, Francesca

Urban Planning, 8, 3, 363-375, Shipping Canals in Transition: Rethinking Spatial, Economic, and Environmental Dimensions From Sea to Hinterland

Ceolin, C.; Schramm, M.; Bodmann, B. E. J.; Vilhena, M. T.; de Q. B.Leite, S.

Kerntechnik. 79(5):430-435

Hirschel J; Division of Neonatal and Intensive Care, Department of Pediatrics, Gynecology and Obstetrics, University Hospitals of Geneva, Geneva, Switzerland.; Barcos-Munoz F; Division of Neonatal and Intensive Care, Department of Pediatrics, Gynecology and Obstetrics, University Hospitals of Geneva, Geneva, Switzerland.; Chalard F; Unit of Pediatric Radiology, Department of Radiology, University Hospitals of Geneva and Faculty of Medicine, University of Geneva, Geneva, Switzerland.; Chiodini F; Therapeutic Tissue Biobank, University Hospitals of Geneva, Geneva, Switzerland.; Epiney M; Obstetrics Unit Department of Obstetrics and Gynecology, University Hospitals of Geneva and Faculty of Medicine, University of Geneva, Geneva, Switzerland.; Fluss J; Pediatric Neurology Unit, University Hospitals of Geneva and Faculty of Medicine, University of Geneva, Geneva, Switzerland.; Rougemont AL; Division of Clinical Pathology, Diagnostic Department, Geneva University Hospitals and Faculty of Medicine, University of Geneva, Geneva, Switzerland. anne-laure.rougemont@hug.ch.

Publisher: Springer International Country of Publication: Germany NLM ID: 9423843 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-2307 (Electronic) Linking ISSN: 09456317 NLM ISO Abbreviation: Virchows Arch Subsets: MEDLINE

Paulet A; Département de Génétique, Hôpital Robert-Debré, Paris, France. alix.paulet@hotmail.fr.; Bennett-Ness C; Centre for Genomic and Experimental Medicine and Simons Initiative for the Developing Brain, Institute of Genetics and Cancer, Edinburgh, Scotland, UK.; Ageorges F; Département de Génétique, Hôpital Robert-Debré, Paris, France.; Trost D; Laboratoire Cerba, Saint-Ouen l'Aumône, France.; Green A; UCD School of Medicine and Medical Science Consultant in Clinical Genetics, Dublin, Ireland.; Goudie D; Regional Genetics Service, NHS Tayside, Dundee, Scotland, UK.; Jewell R; Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, England, UK.; Kraatari-Tiri M; Department of Clinical Genetics, Research unit of Clinical Medicine, Medical Research Center Oulu, Oulu, Finland.; Oulu University Hospital and University of Oulu, Oulu, Finland.; Piard J; Centre de Génétique Humaine, CHU Besançon, Besançon, France.; Coubes C; Service de Génétique Médicale, CHU de Montpellier, Montpellier, France.; Lam W; South-East of Scotland Clinical Genetics Service, General Hospital, Edinburgh, Scotland, UK.; Lynch SA; Clinical Genetics, Children's Health Ireland, Dublin, Ireland.; Groeschel S; Department of Neuropediatrics, University Children's Hospital, Tuebingen, Germany.; Ramond F; Service de Génétique, CHU Saint-Etienne - Hôpital Nord, Saint-Etienne, France.; Fluss J; University Hospitals of Geneva, Geneva, Switzerland.; Fagerberg C; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.; Brasch Andersen C; Human Genetik, Syddansk Universitet, Odense, Denmark.; Varvagiannis K; Service de Médecine Génétique, Hôpitaux universitaires de Genève, Geneva, Switzerland.; Kleefstra T; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.; Center of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands.; Gérard B; Molecular Biology, Nouvel Hôpital Civil, Strasbourg, France.; Fradin M; Service de Génétique Médicale, Hôpital Sud, CHU de Rennes, Rennes, France.; Vitobello A; UMR-Inserm, Génétique des Anomalies du développement, Université de Bourgogne Franche-Comté, Dijon, France.; Tenconi R; Servizio di Genetica Medica, Dipartimento di Pediatra, Padova, Italia.; Denommé-Pichon AS; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Vincent-Devulder A; Génétique Médicale, CHU de Caen, Caen, France.; Haack T; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Marsh JA; MRC Human Genetics Unit, Western General Hospital, University of Edinburgh, Edinburgh, Scotland, UK.; Laulund LW; H C Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.; Grimmel M; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Riess A; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; de Boer E; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.; Padilla-Lopez S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.; Bakhtiari S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.; Ostendorf A; Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital, Colombus, OH, USA.; Department of Pediatrics, The Ohio State University College of Medicine, Colombus, OH, USA.; Zweier C; Department of Human Genetics, Inselspital Bern, University of Bern, 3010, Bern, Switzerland.; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054, Erlangen, Germany.; Smol T; University of Lille, EA7364-RADEME, Medical Genetics Institute, Chu Lille, Lille, France.; Willems M; Medical Genetic Department for Rare Diseases and Personalized Medicine, Reference Center AD SOOR, AnDDI-RARE, Groupe DI, Inserm U1298, INM, Montpellier University, Montpellier, France.; Centre Hospitalier Universitaire de Montpellier, Montpellier, France.; Faivre L; UMR1231 GAD, Inserm, Université de Bourgogne-Franche Comté, Dijon, France.; Centre de Référence Maladies Rares « Anomalies du développement et syndromes malformatifs », Centre de Génétique, FHU-TRANSLAD et Institut GIMI, CHU dijon, Bourgogne, Dijon, France.; Scala M; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Striano P; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Bagnasco I; Division of Child Neuropsychiatry, Martini Hospital, Torino, Italy.; Koboldt D; Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital, Colombus, OH, USA.; Iascone M; Laboratorio Di Genetica Medica, Bergamo, Italy.; Suerink M; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.; Kruer MC; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.; Levy J; Département de Génétique, Hôpital Robert-Debré, Paris, France.; Verloes A; Département de Génétique, Hôpital Robert-Debré, Paris, France.; Abbott CM; Centre for Genomic and Experimental Medicine and Simons Initiative for the Developing Brain, Institute of Genetics and Cancer, Edinburgh, Scotland, UK.; Ruaud L; Département de Génétique, Hôpital Robert-Debré, Paris, France.

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

Chabrier, S. ; Kossorotoff, M.; Chevin, M.; Fluss, J.

In Bulletin de l'Académie Nationale de Médecine May 2021 205(5):490-498