부산대학교 도서관

Wintermark M; Hills NK; de Veber GA; Barkovich AJ; Elkind MSV; Sear K; Zhu G; Leiva-Salinas C; Hou Q; Dowling MM; Bernard TJ; Friedman NR; Ichord RN; Fullerton HJ; Benedict SL; Fox CK; Lo WD; Tan MA; Mackay MT; Kirton A; Hernandez Chavez MI; Humphreys P; Jordan LC; Sultan SM; Rivkin MJ; Rafay MF; Titomanlio L; Kovacevic GS; Yager JY; Amlie-Lefond C; Dlamini N; Condie J; Yeh A; Kneen R; Bjornson BH; Pergami P; Zou LP; Elbers J; Abdalla A; Chan AK; Farooq O; Lim MJ; Carpenter JL; Pavlakis S; Wong VC; Forsyth R

Stroke. 45:3597-3605

Rafay MF; Cortez MA; de Veber GA; Tan-Dy C; Al-Futaisi A; Yoon W; Fallah S; Moore AM; Rafay, Mubeen F; Cortez, Miguel A; de Veber, Gabrielle A; Tan-Dy, Cherrie; Al-Futaisi, Amna; Yoon, Woojin; Fallah, Shafagh; Moore, Aideen M

Stroke (00392499) (STROKE), Jul2009; 40(7): 2402-2407. (6p)

Nursing Clinics of North America (NURS CLIN NORTH AM), 1966 Jun; 1: 275-275. (1p)

Lecoquierre F; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France. francois.lecoquierre@chu-rouen.fr.; Centre de Ressources Biologiques institutionnel du CHU de Rouen - Biothèque filière génétique, Rouen, France. francois.lecoquierre@chu-rouen.fr.; Cassinari K; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Drouot N; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; May A; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Fourneaux S; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Charbonnier F; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Derambure C; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Coutant S; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Saugier-Veber P; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Hoischen A; Department of Human Genetics, Radboud University Medical Center, 6525 GA, Nijmegen, The Netherlands.; Charbonnier C; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Nicolas G; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.

Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE

Aref-Eshghi E; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.; Kerkhof J; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.; Pedro VP; Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON N6A5C1, Canada.; Barat-Houari M; Autoinflammatory and Rare Diseases Unit, Medical Genetic Department for Rare Diseases and Personalized Medicine, Centre Hospitalier Universitaire de Montpellier, 34090 Montpellier, France.; Ruiz-Pallares N; Autoinflammatory and Rare Diseases Unit, Medical Genetic Department for Rare Diseases and Personalized Medicine, Centre Hospitalier Universitaire de Montpellier, 34090 Montpellier, France.; Andrau JC; Institut de Génétique Moléculaire de Montpellier (IGMM), University Montpellier, CNRS-UMR5535, 34090 Montpellier, France.; Lacombe D; Medical Genetics Department, Inserm U1211, Reference Center AD SOOR, AnDDI-RARE, Bordeaux University, Centre Hospitalier Universitaire de Bordeaux, 33076 Bordeaux, France.; Van-Gils J; Medical Genetics Department, Inserm U1211, Reference Center AD SOOR, AnDDI-RARE, Bordeaux University, Centre Hospitalier Universitaire de Bordeaux, 33076 Bordeaux, France.; Fergelot P; Medical Genetics Department, Inserm U1211, Reference Center AD SOOR, AnDDI-RARE, Bordeaux University, Centre Hospitalier Universitaire de Bordeaux, 33076 Bordeaux, France.; Dubourg C; Service de Génétique Moléculaire et Génomique, Centre Hospitalier Universitaire de Rennes, 35000 Rennes, France.; Cormier-Daire V; Department of Medical Genetics, Paris Descartes University, INSERM UMR 1163, Imagine Institute, Necker Enfants Malades Hospital, 75015 Paris, France.; Rondeau S; Department of Medical Genetics, Paris Descartes University, INSERM UMR 1163, Imagine Institute, Necker Enfants Malades Hospital, 75015 Paris, France.; Lecoquierre F; Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, F 76000, Normandy Center for Genomic and Personalized Medicine, 76183 Rouen, France.; Saugier-Veber P; Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, F 76000, Normandy Center for Genomic and Personalized Medicine, 76183 Rouen, France.; Nicolas G; Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, F 76000, Normandy Center for Genomic and Personalized Medicine, 76183 Rouen, France.; Lesca G; Department of Medical Genetics, University Hospital of Lyon, 69007 Lyon, France.; Chatron N; Department of Medical Genetics, University Hospital of Lyon, 69007 Lyon, France.; Sanlaville D; Department of Medical Genetics, University Hospital of Lyon, 69007 Lyon, France.; Vitobello A; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, 15 boulevard du Maréchal de Lattre de Tassigny, 21000, Dijon Cedex, France; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, Dijon University Hospital, 21000 Dijon, France.; Faivre L; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, 15 boulevard du Maréchal de Lattre de Tassigny, 21000, Dijon Cedex, France; Centre de Référence Déficiences Intellectuelles de Causes Rares, CHU Dijon, 21000, Dijon, France.; Thauvin-Robinet C; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, 15 boulevard du Maréchal de Lattre de Tassigny, 21000, Dijon Cedex, France; Centre de Référence Déficiences Intellectuelles de Causes Rares, CHU Dijon, 21000, Dijon, France.; Laumonnier F; UMR 1253, iBrain, Universite de Tours, Inserm, 37200 Tours, France; Centre Hospitalier Universitaire de Tours, Service de Genetique, 37000 Tours, France.; Raynaud M; UMR 1253, iBrain, Universite de Tours, Inserm, 37200 Tours, France; Centre Hospitalier Universitaire de Tours, Service de Genetique, 37000 Tours, France.; Alders M; Amsterdam University Medical Center, University of Amsterdam, Department of Clinical Genetics, Amsterdam Reproduction and Development Research Institute, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.; Mannens M; Amsterdam University Medical Center, University of Amsterdam, Department of Clinical Genetics, Amsterdam Reproduction and Development Research Institute, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.; Henneman P; Amsterdam University Medical Center, University of Amsterdam, Department of Clinical Genetics, Amsterdam Reproduction and Development Research Institute, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.; Hennekam RC; Department of Pediatrics, Academic Medical Center, University of Amsterdam, Amsterdam, 1012 WX, the Netherlands.; Velasco G; Université de Paris, Epigénétique et Destin Cellulaire, CNRS, 75013 Paris, France.; Francastel C; Université de Paris, Epigénétique et Destin Cellulaire, CNRS, 75013 Paris, France.; Ulveling D; Université de Paris, Epigénétique et Destin Cellulaire, CNRS, 75013 Paris, France.; Ciolfi A; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00146 Rome, Italy.; Pizzi S; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00146 Rome, Italy.; Tartaglia M; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00146 Rome, Italy.; Heide S; Department of Genetics, Referral Center for Intellectual Disabilities, APHP Sorbonne University, Pitié Salpêtrière Hospital, 75013 Paris, France.; Héron D; Department of Genetics, Referral Center for Intellectual Disabilities, APHP Sorbonne University, Pitié Salpêtrière Hospital, 75013 Paris, France.; Mignot C; Department of Genetics, Referral Center for Intellectual Disabilities, APHP Sorbonne University, Pitié Salpêtrière Hospital, 75013 Paris, France.; Keren B; Department of Genetics, Referral Center for Intellectual Disabilities, APHP Sorbonne University, Pitié Salpêtrière Hospital, 75013 Paris, France.; Whalen S; Unit of Genetics, APHP Sorbonne University, Trousseau Hospital, 75012 Paris, France.; Afenjar A; Unit of Genetics, APHP Sorbonne University, Trousseau Hospital, 75012 Paris, France.; Bienvenu T; Department of Molecular Genetics, Cochin Hospital, 75014 Paris, France.; Campeau PM; Department of Pediatrics, University of Montreal, Montreal, QC H3T1J4, Canada.; Rousseau J; Department of Pediatrics, University of Montreal, Montreal, QC H3T1J4, Canada.; Levy MA; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada.; Brick L; Genetic Division, Department of Pediatrics, McMaster University, Hamilton, ON L8S4K1, Canada.; Kozenko M; Genetic Division, Department of Pediatrics, McMaster University, Hamilton, ON L8S4K1, Canada.; Balci TB; Department of Pediatrics, Division of Medical Genetics, Western University, London, ON N6A 3K7; Medical Genetics Program of Southwestern Ontario, London Health Sciences Centre, London, ON N6A5W9, Canada.; Siu VM; Department of Pediatrics, Division of Medical Genetics, Western University, London, ON N6A 3K7; Medical Genetics Program of Southwestern Ontario, London Health Sciences Centre, London, ON N6A5W9, Canada.; Stuart A; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.; Kadour M; Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A5W9 Canada; St. Joseph's Health Care London, London, ON N6A5W9 Canada.; Masters J; Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A5W9 Canada; St. Joseph's Health Care London, London, ON N6A5W9 Canada.; Takano K; Center for Medical Genetics, Shinshu University Hospital, 3-1-1 Asahi, Matsumoto, Nagano 3908621, Japan.; Kleefstra T; Department of Human Genetics, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands; Donders Center for Medical Neuroscience, 6525 GA Nijmegen, the Netherlands.; de Leeuw N; Department of Human Genetics, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands; Donders Center for Medical Neuroscience, 6525 GA Nijmegen, the Netherlands.; Field M; Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW 2298, Australia.; Shaw M; School of Medicine, Robinson Research Institute, University of Adelaide, Adelaide, SA 5005, Australia.; Gecz J; School of Medicine, Robinson Research Institute, University of Adelaide, Adelaide, SA 5005, Australia; South Australian Health and Medical Research Institute, Adelaide, SA 5005, Australia.; Ainsworth PJ; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada.; Lin H; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada.; Rodenhiser DI; Children's Health Research Institute, London, ON N6A3K7, Canada; Department of Biochemistry, Western University, London, ON N6A3K7, Canada.; Friez MJ; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Tedder M; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Lee JA; Greenwood Genetic Center, Greenwood, SC 29646, USA.; DuPont BR; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Stevenson RE; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Skinner SA; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Schwartz CE; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Genevieve D; Medical Genetic Department for Rare Diseases and Personalized Medicine, Reference Center AD SOOR, AnDDI-RARE, Groupe DI, Inserm U1183-Institute for Regenerative Medicine and Biotherapy, Montpellier University, Centre Hospitalier Universitaire de Montpellier, 34090 Montpellier, France.; Sadikovic B; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada. Electronic address: Bekim.Sadikovic@lhsc.on.ca.

Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Karanicolas S; Oreopoulos DG; Pylypchuk G; Fenton SS; Cattran DC; Rapoport A; de Veber GA

Publisher: Canadian Medical Association Country of Publication: Canada NLM ID: 0414110 Publication Model: Print Cited Medium: Print ISSN: 0008-4409 (Print) Linking ISSN: 00084409 NLM ISO Abbreviation: Can Med Assoc J Subsets: MEDLINE

Oreopoulos DG; Pitel S; Husdan H; de Veber GA; Rapoport A

Publisher: Canadian Medical Association Country of Publication: Canada NLM ID: 0414110 Publication Model: Print Cited Medium: Print ISSN: 0008-4409 (Print) Linking ISSN: 00084409 NLM ISO Abbreviation: Can Med Assoc J Subsets: MEDLINE

Rubin J; Oreopoulos DG; Lio TT; Mathews R; de Veber GA

Publisher: Karger Country of Publication: Switzerland NLM ID: 0331777 Publication Model: Print Cited Medium: Print ISSN: 1660-8151 (Print) Linking ISSN: 16608151 NLM ISO Abbreviation: Nephron Subsets: MEDLINE

Whiteside CI; Cardella CJ; Yeung H; de Veber GA; Cook GT

Publisher: Dustri-Verlag Dr. Karl Feistle Country of Publication: Germany NLM ID: 0364441 Publication Model: Print Cited Medium: Print ISSN: 0301-0430 (Print) Linking ISSN: 03010430 NLM ISO Abbreviation: Clin Nephrol Subsets: MEDLINE

Cardella CJ; de Veber GA; Hollenberg C; Marshall WJ; Seaver R; Robinette MA; Lindberg MC; Stiller CR

Publisher: Elsevier Science Inc Country of Publication: United States NLM ID: 0243532 Publication Model: Print Cited Medium: Print ISSN: 0041-1345 (Print) Linking ISSN: 00411345 NLM ISO Abbreviation: Transplant Proc Subsets: MEDLINE

Robson MD; Oreopoulos DG; Clayton S; Izatt S; Rapoport A; de Veber GA

Publisher: Pitman Publishing Country of Publication: England NLM ID: 0355210 Publication Model: Print Cited Medium: Print ISSN: 0071-2736 (Print) Linking ISSN: 00712736 NLM ISO Abbreviation: Proc Eur Dial Transplant Assoc Subsets: MEDLINE

Velentzas C; Oreopoulos DG; Meindok H; Meema HE; Rabinovich S; Jones M; Sutton D; Rapoport A; de Veber GA

Publisher: Georgetown University Hospital. Department Of Medicine Country of Publication: United States NLM ID: 0432324 Publication Model: Print Cited Medium: Print ISSN: 0094-6044 (Print) Linking ISSN: 00946044 NLM ISO Abbreviation: Proc Clin Dial Transplant Forum Subsets: MEDLINE

Karanicolas S; Oreopoulos DG; Izatt S; Shimizu A; Manning RF; Sepp H; de Veber GA; Darby T

Publisher: Massachusetts Medical Society Country of Publication: United States NLM ID: 0255562 Publication Model: Print Cited Medium: Print ISSN: 0028-4793 (Print) Linking ISSN: 00284793 NLM ISO Abbreviation: N Engl J Med Subsets: MEDLINE

Oreopoulos DG; Jones M; Devine H; McCleary P; Fenton S; de Veber GA

Publisher: Georgetown University Hospital. Department Of Medicine Country of Publication: United States NLM ID: 0432324 Publication Model: Print Cited Medium: Print ISSN: 0094-6044 (Print) Linking ISSN: 00946044 NLM ISO Abbreviation: Proc Clin Dial Transplant Forum Subsets: MEDLINE

Schatz DL; Sheppard RH; Steiner G; Chandarlapaty CS; de Veber GA

Publisher: Oxford University Press Country of Publication: United States NLM ID: 0375362 Publication Model: Print Cited Medium: Print ISSN: 0021-972X (Print) Linking ISSN: 0021972X NLM ISO Abbreviation: J Clin Endocrinol Metab Subsets: MEDLINE

Oreopoulos DG; Bigelow P; Devine H; De Veber GA

Publisher: American Medical Association Country of Publication: United States NLM ID: 7501160 Publication Model: Print Cited Medium: Print ISSN: 0098-7484 (Print) Linking ISSN: 00987484 NLM ISO Abbreviation: JAMA Subsets: MEDLINE