부산대학교 도서관

Besnard, Philippe; Durkheim, E.

Revue française de sociologie, 1976 Apr 01. 17(2), 190-196.

Ichimura, Atsuhiko; Hirasawa, Akira; Poulain-Godefroy, Odile; Bonnefond, Amélie; Hara, Takafumi; Yengo, Loïc; Kimura, Ikuo; Leloire, Audrey; Liu, Ning; Iida, Keiko; Choquet, Hélène; Besnard, Philippe; Lecoeur, Cécile; Vivequin, Sidonie; Ayukawa, Kumiko; Takeuchi, Masato; Ozawa, Kentaro; Tauber, Maithé; Maffeis, Claudio; Morandi, Anita; Buzzetti, Raffaella; Elliott, Paul; Pouta, Anneli; Jarvelin, Marjo-Riitta; Körner, Antje; Kiess, Wieland; Pigeyre, Marie; Caiazzo, Roberto; Van Hul, Wim; Van Gaal, Luc; Horber, Fritz; Balkau, Beverley; Lévy-Marchal, Claire; Rouskas, Konstantinos; Kouvatsi, Anastasia; Hebebrand, Johannes; Hinney, Anke; Scherag, Andre; Pattou, François; Meyre, David; Koshimizu, Taka-aki; Wolowczuk, Isabelle; Tsujimoto, Gozoh; Froguel, Philippe

Nature. Mar 15, 2012 483(7389):350-354

Revue française de sociologie 33(2):288

Sociology. Aug83, Vol. 17 Issue 3, p410-412. 3p.

In International Journal of Approximate Reasoning 2007 45(2):308-320

Cuinat S; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France. Electronic address: silvestre.cuinat@chu-nantes.fr.; Nizon M; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France.; Isidor B; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France.; Stegmann A; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; van Jaarsveld RH; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; van Gassen KL; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; van der Smagt JJ; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Volker-Touw CML; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Holwerda SJB; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Terhal PA; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Schuhmann S; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.; Vasileiou G; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.; Khalifa M; Genetic Department, Dubai Health Authority, Latifa Women and Children Hospital, Dubai, United Arab Emirates.; Nugud AA; Genetic Department, Dubai Health Authority, Latifa Women and Children Hospital, Dubai, United Arab Emirates.; Yasaei H; Dubai Genetics Center, Pathology and Genetics Department, Dubai Health Authority, Dubai, United Arab Emirates.; Ousager LB; Department of Clinical Genetics & Human Genetics, Odense University Hospital, University of Southern Denmark, Odense, Denmark; Department of Clinical Research, Odense University Hospital, University of Southern Denmark, Odense, Denmark.; Brasch-Andersen C; Department of Clinical Genetics & Human Genetics, Odense University Hospital, University of Southern Denmark, Odense, Denmark; Department of Clinical Research, Odense University Hospital, University of Southern Denmark, Odense, Denmark.; Deb W; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France.; Besnard T; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France.; Simon MEH; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Amsterdam KH; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Verbeek NE; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Matalon D; Department of Pediatric, Division of Medical Genetics, Stanford University and Health Care, Palo Alto, CA.; Dykzeul N; Department of Pediatric, Division of Medical Genetics, Stanford University and Health Care, Palo Alto, CA.; White S; Department of Pediatric, Division of Medical Genetics, Stanford University and Health Care, Palo Alto, CA.; Spiteri E; Department of Pediatric, Division of Medical Genetics, Stanford University and Health Care, Palo Alto, CA.; Devriendt K; Center for Human Genetics, University Hospital Leuven, KU Leuven, O&N I Herestraat 49, Leuven, Belgium.; Boogaerts A; Center for Human Genetics, University Hospital Leuven, KU Leuven, O&N I Herestraat 49, Leuven, Belgium.; Willemsen M; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Brunner HG; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Sinnema M; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; De Vries BBA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Gerkes EH; University Medical Center Groningen, Department of Genetics, University of Groningen, Groningen, The Netherlands.; Pfundt R; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Izumi K; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.; Krantz ID; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.; Xu ZL; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.; Murrell JR; Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA.; Valenzuela I; Department of Clinical and Molecular Genetics, Hospital Vall d'Hebron, Barcelona, Spain.; Cusco I; Department of Clinical and Molecular Genetics, Hospital Vall d'Hebron, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, Spain.; Rovira-Moreno E; Department of Clinical and Molecular Genetics, Hospital Vall d'Hebron, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, Spain.; Yang Y; AiLife Diagnostics, Pearland, TX.; Bizaoui V; Clinical Genetics and Neurodevelopmental Disorders, Centre Hospitalier de l'Estran, Pontorson, France.; Patat O; Department of Medical Genetics, Toulouse University Hospital, Toulouse, France.; Faivre L; Centre de référence Anomalies du Développement et Syndromes malformatifs, FHU-TRANSLAD, GAD, CHU Dijon et Université de Bourgogne, Dijon, France; Inserm UMR1231, GAD, Université de Bourgogne, Dijon, France.; Tran-Mau-Them F; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; Inserm UMR1231, GAD, Université de Bourgogne, Dijon, France.; Vitobello A; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; Inserm UMR1231, GAD, Université de Bourgogne, Dijon, France.; Denommé-Pichon AS; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; Inserm UMR1231, GAD, Université de Bourgogne, Dijon, France.; Philippe C; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; Inserm UMR1231, GAD, Université de Bourgogne, Dijon, France.; Bezieau S; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France.; Cogné B; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France. Electronic address: benjamin.cogne@chu-nantes.fr.

Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Revue française de sociologie, 1976 Apr 01. 17(2), 165-180.

Digestive Diseases and Sciences. January, 2013, Vol. 58 Issue 1, p5, 3 p.

Revue française de sociologie, 1976 Apr 01. 17(2), 313-341.

Besnard, Philippe; Essyad, Marie-France

Revue française de sociologie, 1976 Apr 01. 17(2), 343-353.