학술논문

발행년
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(예 : 2010-2015)
'학술논문' 에서 검색결과 8건 | 목록 1~10
Academic Journal
Dupont MA; Laboratory of Hereditary Kidney Diseases, INSERM, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Humbert C; Laboratory of Hereditary Kidney Diseases, INSERM, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Huber C; Laboratory of Molecular and Physiopathological bases of osteochondrodysplasia, INSERM, Paris, France.; Department of Genetics, Reference Centre for Skeletal Dysplasia, Assistance Publique - Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Siour Q; Laboratory of Molecular and Physiopathological bases of osteochondrodysplasia, INSERM, Paris, France.; Department of Genetics, Reference Centre for Skeletal Dysplasia, Assistance Publique - Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Guerrera IC; Proteomics Platform 3P5-Necker, Paris Descartes-Sorbonne Paris Cité University, Structure Fédérative de Recherche Necker, INSERM US24/CNRS UMS3633, Paris, France.; Jung V; Proteomics Platform 3P5-Necker, Paris Descartes-Sorbonne Paris Cité University, Structure Fédérative de Recherche Necker, INSERM US24/CNRS UMS3633, Paris, France.; Christensen A; Department of Structural Cell Biology, Max-Planck-Institute of Biochemistry, Martinsried, Germany.; Pouliet A; Genomics Core Facility, Imagine Institute and Structure Fédérative de Recherche Necker, INSERM UMR1163 and INSERM US24/CNRS UMS3633, Paris Descartes-Sorbonne Paris Cité University, Paris, France.; Garfa-Traoré M; Cell Imaging Platform UMS 24, Structure Fédérative de Recherche Necker, Inserm US24/CNRS UMS3633, Paris, France.; Nitschké P; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Bioinformatics Core Facility, Paris Descartes-Sorbonne Paris Cité University, Paris, France.; Injeyan M; The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.; Millar K; The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.; Chitayat D; The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.; Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Shannon P; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.; Girisha KM; Department of Medical Genetics, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.; Shukla A; Department of Medical Genetics, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.; Mechler C; Assistance Publique - Hôpitaux de Paris, Louis Mourier Hospital, Colombes, France.; Lorentzen E; Department of Structural Cell Biology, Max-Planck-Institute of Biochemistry, Martinsried, Germany.; Benmerah A; Laboratory of Hereditary Kidney Diseases, INSERM, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Cormier-Daire V; Laboratory of Molecular and Physiopathological bases of osteochondrodysplasia, INSERM, Paris, France.; Department of Genetics, Reference Centre for Skeletal Dysplasia, Assistance Publique - Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Jeanpierre C; Laboratory of Hereditary Kidney Diseases, INSERM, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Saunier S; Laboratory of Hereditary Kidney Diseases, INSERM, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Delous M; Laboratory of Hereditary Kidney Diseases, INSERM, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.
Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Academic Journal
Ghosh S; IRIBHM, Campus Erasme, ULB Bâtiment C, Bruxelles, Belgium.; Huber C; Department of Medical Genetics, Reference Center for Skeletal Dysplasia, INSERM UMR 1163, Laboratory of Molecular and Physiopathological Bases of Osteochondrodysplasia, Paris Descartes-Sorbonne Paris Cité University, AP-HP, Institut Imagine, Paris, France.; Hôpital Universitaire Necker-Enfants Malades, Paris, France.; Siour Q; Department of Medical Genetics, Reference Center for Skeletal Dysplasia, INSERM UMR 1163, Laboratory of Molecular and Physiopathological Bases of Osteochondrodysplasia, Paris Descartes-Sorbonne Paris Cité University, AP-HP, Institut Imagine, Paris, France.; Hôpital Universitaire Necker-Enfants Malades, Paris, France.; Sousa SB; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalare Universitário de Coimbra, Coimbra, Portugal.; Wright M; Northern Genetics Service, Newcastle-upon-Tyne Hospitals, Newcastle- upon-Tyne, UK.; Cormier-Daire V; Department of Medical Genetics, Reference Center for Skeletal Dysplasia, INSERM UMR 1163, Laboratory of Molecular and Physiopathological Bases of Osteochondrodysplasia, Paris Descartes-Sorbonne Paris Cité University, AP-HP, Institut Imagine, Paris, France.; Hôpital Universitaire Necker-Enfants Malades, Paris, France.; Erneux C; IRIBHM, Campus Erasme, ULB Bâtiment C, Bruxelles, Belgium.
Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Conference
Beekmann, M.Borbon, A.Afif, C.Ait-Helal, V.Aumont, B.Chevailler, S.Chelin, P.Coll, I.Doussin, J.F.Durand-Jolibois, R.Mac Leod, H.Michoud, V.Miet, K.Grand, N.Perrier, S.Petetin, H.Raventos, T.Schmechtig, C.Siour, G.Viatte, C.Zhang, Q.Baltensperger, U.De Carlo, P.Prevot, A.Crippa, M.Mohr, C.Laborde, M.Gysel, M.Chirico, R.Heringa, M.Sciare, J.Gros, V.Chazette, P.Bressi, M.Royer, P.Sarda-Esteve, R.Baklanov, A.Lawrence, M.Lopez, M.Drewnick, F.Schneider, J.Brands, M.Bormann, S.Dzepina, K.Freutel, F.Gallavardin, S.Klimach, T.Marbach, T.Shaiganfar, R.Von Der Weiden, S.L.Wagner, T.Zorn, S.Pandis, S.Kostenidou, V.Psichoudaki, M.Gomes, L.Tulet, P.Wiedensohler, A.Poulain, L.Kamilli, K.Birmli, W.Schwarzenboeck, A.Sellegri, K.Colomb, A.Pichon, J.M.Fernay, E.Jaffrezo, J.L.Laj, P.Butet, A.Bourdon, A.Mathieu, E.Perrin, T.Wenger, J.Healy, R.Connor, I.O.Mc Gillicuddy, E.Alto, P.Jalkanen, J.P.Kulmala, M.Lameloise, P.Ghersi, V.Sanchez, O.Kauffman, A.Marfaing, H.Honoré, C.Chiappini, L.Favez, O.Melleux, F.Aymoz, G.Bessagnet, B.Rouil, L.Rossignol, S.Haeffelin, M.Pietras, C.Dupont, J.C.Kukui, S.Dieudonné, E.Ravetta, F.Raut, J.C.Ancellet, G.Goutail, F.Besombes, J.L.Marchand, N.Le Moullec, Y.Cuesta, J.Te, Y.Laccoge, N.Lolli, S.Sauvage, L.Loannec, S.Ptak, D.Schmidt, A.Conil, S.Boquet, M.Held, A.
In: HARMO 2010 - Proceedings of the 13th International Conference on Harmonisation within Atmospheric Dispersion Modelling for Regulatory Purposes. (HARMO 2010 - Proceedings of the 13th International Conference on Harmonisation within Atmospheric Dispersion Modelling for Regulatory Purposes, 2010, :519-523)
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[검색어] Siour, Q.
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