학술논문

발행년
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(예 : 2010-2015)
'학술논문' 에서 검색결과 2,153건 | 목록 1~10
Conference
2024 IEEE Symposium on Security and Privacy (SP) SP Symposium on Security and Privacy (SP), 2024 IEEE. :3497-3514 May, 2024
Academic Journal
Heide S; Department of Genetics and Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Assistance Publique-Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, 75013, France, Paris, France solveig.heide@aphp.fr.; Argilli E; Department of Neurology, University of California San Francisco Division of Hospital Medicine, San Francisco, California, USA.; Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, California, USA.; Valence S; Department of Neuropediatry & Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Hopital Armand-Trousseau, Paris, France.; Boutaud L; Genomic medicine of rare diseases, UF MP5, Hopital universitaire Necker-enfants Malades, Assistance Publique Hôpitaux de Paris, Paris, France.; Roux N; Genomic medicine of rare diseases, UF MP5, Hopital universitaire Necker-enfants Malades, Assistance Publique Hôpitaux de Paris, Paris, France.; Mignot C; Department of Genetics and Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Assistance Publique-Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, 75013, France, Paris, France.; Nava C; Department of Genetics, Unit of Developmental Genomics, AP-HP.Sorbonne Université, Pitié-Salpêtrière Hospital, Paris, France.; Keren B; Department of Genetics, Unit of Developmental Genomics, AP-HP.Sorbonne Université, Pitié-Salpêtrière Hospital, Paris, France.; Giraudat K; Department of Neuropediatry & Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Hopital Armand-Trousseau, Paris, France.; Faudet A; Department of Genetics and Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Assistance Publique-Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, 75013, France, Paris, France.; Gerasimenko A; Department of Genetics and Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Assistance Publique-Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, 75013, France, Paris, France.; Garel C; Department of pediatric and prenatal imaging, Armand-Trousseau Hospital, Sorbonne Université, Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.; Blondiaux E; Department of pediatric and prenatal imaging, Armand-Trousseau Hospital, Sorbonne Université, Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.; Rastetter A; Paris Brain Institute (ICM Institut du Cerveau), Sorbonne Université, INSERM UMR S 1127, Paris, France.; Grevent D; Radiology Department, Hopital universitaire Necker-enfants Malades, Paris, France.; EA fetus 7328 and LUMIERE Platform, Université de Paris, Paris, France.; Le C; Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, California, USA.; Department of Neurology, University of California, Institute of Human Genetics and Weill Institute for Neurosciences, San Francisco, California, USA.; Mackenzie L; Department of Neuroscience, Washington University in St Louis School of Medicine, St Louis, Missouri, USA.; Richards L; Department of Neuroscience, Washington University in St Louis School of Medicine, St Louis, Missouri, USA.; Queensland Brain Institute, University of Queensland, Brisbane, Queensland, Australia.; Attié-Bitach T; Genomic medicine of rare diseases, UF MP5, Hopital universitaire Necker-enfants Malades, Assistance Publique Hôpitaux de Paris, Paris, France.; Depienne C; Institute of Human Genetics, University Hospital Essen, Universitu Duisburg-Essen, Essen, Germany.; Sherr E; Department of Neurology, University of California San Francisco Division of Hospital Medicine, San Francisco, California, USA.; Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, California, USA.; Héron D; Department of Genetics and Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Assistance Publique-Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, 75013, France, Paris, France.
Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Academic Journal
Endocrine Reviews. April, 2023, Vol. 44 Issue 2, p254, 27 p.
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[검색어] Sherr, E
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