부산대학교 도서관

Piarroux J; Department of Pediatric Neurology, Gui de Chauliac University Hospital, Montpellier, France.; Dimopoulou E; Department of Pediatric Neurology, Gui de Chauliac University Hospital, Montpellier, France.; Taieb G; University of Montpellier, CNRS (IGF), Department of Neurology, Montpellier, University Hospital 34295 Montpellier, France.; Souvannanorath S; Reference center for neuromuscular diseases, Henri-Mondor University Hospital, Assistance publique-Hôpitaux de Paris, Créteil, France.; Roze E; Department of Neurology, Salpêtrière Hospital, Sorbonne University and Assistance Publique - Hôpitaux de Paris, Paris, France.; Lion-François L; Department of Pediatric Neurology, Lyon University Hospital, Bron, France.; Spitz MA; Department of Pediatry, Strasbourg University Hospitals, Strasbourg, France.; Broussolle E; Research Unit UMR 5229, Marc-Jeannerod Institute of Cognitive Science, French National Center for Scientific Research (CNRS), University of Lyon, Bron, France.; Department of Neurology C, Civil Hospices of Lyon, Pierre-Wertheimer Neurological Hospital, Bron, France.; Faculty of Medicine Lyon-Sud Charles-Mérieux, University of Lyon, Oullins, France.; Laurencin C; Department of Neurology C, Civil Hospices of Lyon, Pierre-Wertheimer Neurological Hospital, Bron, France.; Lyon Neuroscience Research Center (CRNL), INSERM U1028, CNRS UMR5292, University Lyon 1, Lyon F-69000, France.; Chanson JB; Department of Neurology, Strasbourg University Hospitals, Strasbourg, France and Reference centre for neuromuscular diseases Nord/Est/Ile-de-France, France.; Belleville-Goffeney J; Departement of Pediatric Neurology, Jean-Minjoz University Hospital, Besançon, France.; François-Heude MC; Department of Pediatric Neurology, Gui de Chauliac University Hospital, Montpellier, France.; Meyer P; Department of Pediatric Neurology, Gui de Chauliac University Hospital, Montpellier, France.; Khalil M; Clinical Investigation Center, Montpellier University Hospital, France. INSERM, CIC1411, Montpellier, France.; Dereure M; Clinical Research and Epidemiology Unit, La Colombière University Hospital, Montpellier, France.; Doummar D; Department of Pediatric Neurology and developmental pathologies, Sorbonne University and Trousseau University Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France, APHP. SU, FHU I2D2, F-75012, Paris, France.; Chevassus H; Clinical Investigation Center, Montpellier University Hospital, France. INSERM, CIC1411, Montpellier, France.; Apartis E; Department of Neurophysiology, Saint-Antoine Hospital, Assistance Publique-Hôpitaux de Paris, INSERM U1127, CNRS UMR7225, UM75, ICM, 75013 Paris, France.; Roubertie A; Department of Pediatric Neurology, Gui de Chauliac University Hospital, Montpellier, France.; Institute for Neurosciences of Montpellier, INSERM U 1298, University of Montpellier, Montpellier, France.

Publisher: Ubiquity Press Country of Publication: England NLM ID: 101569493 Publication Model: eCollection Cited Medium: Internet ISSN: 2160-8288 (Electronic) Linking ISSN: 21608288 NLM ISO Abbreviation: Tremor Other Hyperkinet Mov (N Y) Subsets: MEDLINE

Piard, J.; Moris-Rosendahl, D. J.; Putoux, A.; Delplancq, G.; Cabrol, C.; Goffeney, J. Belleville; Pasquier, L.; Brischoux-Boucher, E.; Wollnik, B.; Yigit, G.; Albrecht, B.; Lesca, G.; Villard, Laurent; Edery, P.; Sanlaville, D.; Streichenberger, N.; Altuzarra, C.; Harms, F. L.; Kutsche, K.; van Maldergem, L.

Belleville Goffeney, J.; Paris, C.; Bernard, E.; Boucher, E.; Billon Grand, N.C.; Pastor Harper, D.; Ridley, A.; Burglen, L.; Amsallem, D.

European Journal of Paediatric Neurology. 21:e44-e44

Engel C; Centre de Génétique Humaine, Centre Hospitalier Régional Universitaire, Université de Franche-Comté, Besançon, France. cengel@chu-besancon.fr.; Valence S; Service de Neurologie Pédiatrique, Hôpital Armand Trousseau, APHP Sorbonne Université, Paris, France.; Delplancq G; Centre de Génétique Humaine, Centre Hospitalier Régional Universitaire, Université de Franche-Comté, Besançon, France.; Maroofian R; Department of Neuromuscular Diseases UCL Queen Square Institute of Neurology, University College London, London, UK.; Accogli A; Department of Specialized Medicine, Division of Medical Genetics, McGill University Health Centre, Montreal, QC, Canada.; Agolini E; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Alkuraya FS; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Baglioni V; Department of Human Neurosciences, Institute of Child and Adolescent Neuropsychiatry, Sapienza University of Rome, Rome, Italy.; Bagnasco I; Division of Neuropsychiatry, Epilepsy Center for Children, Martini Hospital, 10141, Turin, Italy.; Becmeur-Lefebvre M; Service de Génétique Clinique, CHR d'Orléans, Orléans, France.; Bertini E; Unit of Neuromuscular and Neurodegenerative Disorders, Department of Neurosciences, Bambino Gesù Children's Hospital IRCCS, Rome, Italy.; Borggraefe I; Department of Pediatric Neurology, Developmental Medicine and Social Pediatrics, University of Munich, 80337, Munich, Germany.; Brischoux-Boucher E; Centre de Génétique Humaine, Centre Hospitalier Régional Universitaire, Université de Franche-Comté, Besançon, France.; Bruel AL; UMR 1231 GAD, Inserm, Université de Bourgogne Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Brusco A; Department of Medical Sciences, University of Torino, 10126, Turin, Italy.; Bubshait DK; Department of Pediatrics, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.; Cabrol C; Centre de Génétique Humaine, Centre Hospitalier Régional Universitaire, Université de Franche-Comté, Besançon, France.; Cilio MR; Department of Pediatrics, Division of Pediatric Neurology Saint-Luc University Hospital, and Institute of Neuroscience (IoNS), Catholic University of Louvain, Brussels, Belgium.; Cornet MC; Department of Pediatrics, Division of Neonatology, University of California San Francisco, San Francisco, CA, USA.; Coubes C; Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Montpellier, France.; Danhaive O; Division of Neonatology, Saint-Luc university Hospital, and Institut of Clinical and Experimental Research (IREC), Bruxelles, Belgium.; Delague V; Aix Marseille Univ, INSERM, Marseille Medical Genetics Center, MMG, Marseille, France.; Denommé-Pichon AS; UMR 1231 GAD, Inserm, Université de Bourgogne Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Di Giacomo MC; Medical Genetics Service and Laboratory of Cytogenetics, SIC Anatomia Patologica, 'San Carlo' Hospital, 85100, Potenza, Italy.; Doco-Fenzy M; CHU Reims, Service de Génétique, Reims, France.; CHU de Nantes, service de génétique médicale, Nantes, France.; L'institut du thorax, INSERM, UNIV Nantes, Nantes, France.; Engels H; Institute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.; Cremer K; Institute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.; Gérard M; Clinical Genetics, Côte de Nacre University Hospital Center, Caen, France.; Gleeson JG; University of California San Diego, Department of Neurosciences, Rady Children's Institute for Genomic Medicine, San Diego, CA, 92037, USA.; Heron D; Department of Genetics, Pitié-Salpêtrière Hospital, AP-HP, Sorbonne University, Paris, France.; Goffeney J; Service de neuropédiatrie, Centre Hospitalier Régional Universitaire, Université de Franche-Comté, Besançon, France.; Guimier A; Service de Médecine Génomique des Maladies Rares, Hôpital Necker Enfants Malades, Institut Imagine et Université Paris-Cité, Paris, France.; Harms FL; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Houlden H; Department of Neuromuscular Diseases UCL Queen Square Institute of Neurology, University College London, London, UK.; Iacomino M; Unit of Medical Genetics, IRCCS Instituto Giannina Gaslini, Genova, Italy.; Kaiyrzhanov R; Department of Neuromuscular Diseases UCL Queen Square Institute of Neurology, University College London, London, UK.; Kamien B; Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, WA, 6008, Australia.; Karimiani EG; Department of Molecular Genetics, Next Generation Genetic Polyclinic, Mashhad, Iran.; Molecular and Clinical Sciences Institute, St. George's, University of London, Cranmer Terrace, London, SW17 0RE, UK.; Kraus D; Department of Neurology, Schneider Children's Medical Center of Israel, Petah Tiqva, Israel.; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, 6997801, Israel.; Kuentz P; UMR 1231 GAD, Inserm, Université de Bourgogne Franche Comté, Dijon, France.; Oncobiologie Génétique Bioinformatique, PCBio, CHU Besançon, Besançon, France.; Kutsche K; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Lederer D; Institute for Pathology and Genetics, 6040, Gosselies, Belgium.; Massingham L; Division of Medical Genetics, Department of Pediatrics, Hasbro Children's Hospital, Providence, RI, USA.; Mignot C; APHP, Sorbonne Université, Département de Génétique, Paris, France.; Centre de Référence Déficiences Intellectuelles de Causes Rares, GH Pitié-Salpêtrière/Hôpital Armand Trousseau, Paris, France.; Morris-Rosendahl D; Clinical Genetics and Genomics, Royal Brompton and Harefield NHS Foundation Trust, London, UK.; NHLI, Imperial College London, London, UK.; Nagarajan L; Department of Neurology, Perth Children's Hospital, Nedlands, WA, Australia.; University of Western Australia, Nedlands, WA, Australia.; Odent S; Service de Génétique Clinique, Centre Référence 'Déficiences Intellectuelles de causes rares' (CRDI), Centre Référence Anomalies du développement (CLAD-Ouest), CHU Rennes, Univ Rennes, Rennes, France.; Ormières C; Service de Médecine Génomique des Maladies Rares, Hôpital Necker Enfants Malades, Institut Imagine et Université Paris-Cité, Paris, France.; Partlow JN; Division of Genetics and Genomics and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.; Pasquier L; Service de Génétique Clinique, Centre Référence 'Déficiences Intellectuelles de causes rares' (CRDI), Centre Référence Anomalies du développement (CLAD-Ouest), CHU Rennes, Univ Rennes, Rennes, France.; Penney L; Department of Pediatrics, IWK Health Centre, Dalhousie University, Halifax, NS, Canada.; Philippe C; UMR 1231 GAD, Inserm, Université de Bourgogne Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Piccolo G; UOSD Neuro-oncology, IRCCS Giannina Gaslini, Genova, Italy.; Poulton C; Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, WA, 6008, Australia.; Putoux A; Hospices Civils de Lyon, Service de Génétique, Bron, France.; Équipe GENDEV, Centre de Recherche en Neurosciences de Lyon, INSERM U1028 CNRS UMR5292, Université Claude Bernard Lyon 1, Lyon, France.; Rio M; Service de Médecine Génomique des Maladies Rares, Hôpital Necker Enfants Malades, Institut Imagine et Université Paris-Cité, Paris, France.; Rougeot C; Hôpital Femme Mère Enfant, Service de Neuropédiatrie, Bron, France.; Salpietro V; Department of Neuromuscular Diseases UCL Queen Square Institute of Neurology, University College London, London, UK.; IRCCS Giannina Gaslini Institute, Genova, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy.; Scheffer I; Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, VIC, Australia.; Royal Children's Hospital, Florey Institute and Murdoch Children's Research Institute, Melbourne, VIC, Australia.; Schneider A; Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, VIC, Australia.; Srivastava S; Department of Neurology, Boston Children's Hospital, Boston, MA, USA.; Straussberg R; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, 6997801, Israel.; Striano P; IRCCS Giannina Gaslini Institute, Genova, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy.; Valente EM; Department of Molecular Medicine, University of Pavia, Pavia, Italy.; Neurogenetics Research Center, IRCCS Mondino Foundation, Pavia, Italy.; Venot P; Neonatal Intensive Care Unit, Institut Alix de Champagne, Reims, France.; Villard L; Aix Marseille Univ, INSERM, Marseille Medical Genetics Center, MMG, Marseille, France.; Département de Génétique Médicale, AP-HM, Hôpital d'Enfants de La Timone, Marseille, France.; Vitobello A; UMR 1231 GAD, Inserm, Université de Bourgogne Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Wagner J; Department of Pediatric Neurology, Developmental Medicine and Social Pediatrics, University of Munich, 80337, Munich, Germany.; Wagner M; Department of Pediatric Neurology, Developmental Medicine and Social Pediatrics, University of Munich, 80337, Munich, Germany.; Institute for Neurogenomics, Helmholtz Center Munich, Neuherberg, Germany.; Institute of Human Genetics, School of Medicine, Technical University Munich, Munich, Germany.; Zaki MS; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.; Zara F; IRCCS Giannina Gaslini Institute, Genova, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy.; Lesca G; Hospices Civils de Lyon, Service de Génétique, Bron, France.; Pathophysiology and Genetics of Neuron and Muscle (PGNM, UCBL - CNRS UMR5261 - INSERM U1315), Université Claude Bernard Lyon 1, Lyon, France.; Yassaee VR; Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Miryounesi M; Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Hashemi-Gorji F; Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Beiraghi M; Department of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.; Ashrafzadeh F; Department of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.; Galehdari H; Department of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.; Walsh C; Division of Genetics and Genomics and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.; Novelli A; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Tacke M; Department of Pediatric Neurology, Developmental Medicine and Social Pediatrics, University of Munich, 80337, Munich, Germany.; Sadykova D; Astana Medical University, Nur-Sultan, Kazakhstan.; Maidyrov Y; S. D. Asfendiyarov Kazakh National Medical University Almaty, Almaty, Kazakhstan.; Koneev K; Department of Neurology and Neurosurgery, Asfendiyarov Kazakh National Medical University, Almaty, 050000, Kazakhstan.; Shashkin C; Department of Neurology, The International Institute of Postraduate Education, Almaty, Kazakhstan.; Capra V; Unit of Medical Genetics, IRCCS Instituto Giannina Gaslini, Genova, Italy.; Zamani M; Department of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.; Van Maldergem L; Centre de Génétique Humaine, Centre Hospitalier Régional Universitaire, Université de Franche-Comté, Besançon, France.; Burglen L; Centre de Référence des Malformations et Maladies Congénitales du Cervelet, Département de Génétique, AP-HP, Sorbonne Université, Hôpital Trousseau, Paris, France.; Piard J; Centre de Génétique Humaine, Centre Hospitalier Régional Universitaire, Université de Franche-Comté, Besançon, France.; UMR 1231 GAD, Inserm, Université de Bourgogne Franche Comté, Dijon, 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

R. Charollais; J. Belleville-Goffeney; R. Vieux; F. Aubin; E. Puzenat

Annales de Dermatologie et de Vénéréologie. 145:S258

J M, Berg; N W, Goffeney

Methods in enzymology. 276

J. Goffeney; P. Dumont; F. Neumann; R. Chelabi; A. Comte; D. Amsallem; C. Altuzarra

Archives de Pédiatrie. 21:782

Goffeney, A.; Morel, V.; Loe-Mie, Y.; Cossec, J.-C.; Seeler, J.-S.; Dejean, A.; Hendriks, I.A.; Nielsen, M.L.; Charon, F.; Noordermeer, D.

In: Nucleic Acids Research. (Nucleic Acids Research, 12 August 2025, 53(14))

Goffeney N; Department of Radiology, School of Medicine, Johns Hopkins University, 217 Traylor Building, 720 Rutland Avenue, Baltimore, MD 21205, USA.; Bulte JW; Duyn J; Bryant LH Jr; van Zijl PC

Publisher: American Chemical Society Country of Publication: United States NLM ID: 7503056 Publication Model: Print Cited Medium: Print ISSN: 0002-7863 (Print) Linking ISSN: 00027863 NLM ISO Abbreviation: J Am Chem Soc Subsets: MEDLINE

Schmidt, G. S.; Goffeney, J.; Willis, R.

NRL Review; 2007, p217-219, 3p

Kossorotoff M; Assistance publique-Hôpitaux de Paris, French Center for Pediatric Stroke, France.; Pediatric Neurology Department, Assistance publique-Hôpitaux de Paris, Inserm, Hôpital Necker-Enfants malades, Paris, France.; Kerleroux B; Pediatric Radiology Department, Assistance publique-Hôpitaux de Paris, Hôpital Necker-Enfants malades, Paris, France.; GHU Paris Psychiatrie et Neurosciences, CH Sainte-Anne, Inserm, Université de Paris Cité, Institut de psychiatrie et neurosciences de Paris, Service d'imagerie morphologique et fonctionnelle, UMRS1266, Paris, France.; Boulouis G; Assistance publique-Hôpitaux de Paris, French Center for Pediatric Stroke, France.; Pediatric Radiology Department, Assistance publique-Hôpitaux de Paris, Hôpital Necker-Enfants malades, Paris, France.; Neuroradiology, Tours University, CHRU Bretonneau, Tours, France.; Husson B; Assistance publique-Hôpitaux de Paris, French Center for Pediatric Stroke, France.; Pediatric Radiology Department, Assistance publique-Hôpitaux de Paris, Université de Paris-Saclay, Hôpital Bicêtre, le Kremlin-Bicêtre, France.; Tran Dong K; Assistance publique-Hôpitaux de Paris, French Center for Pediatric Stroke, France.; Eugene F; Neuroradiology, Rennes University, CHU de Rennes, Rennes, France.; Damaj L; Pediatric Department, Rennes University, CHU de Rennes, Rennes, France.; Ozanne A; Assistance publique-Hôpitaux de Paris, French Center for Pediatric Stroke, France.; Department of Interventional Neuroradiology Neuro Brain Vascular Center, Assistance publique-Hôpitaux de Paris, Paris-Saclay University, Hôpital Bicêtre, le Kremlin-Bicêtre, France.; Bellesme C; Pediatric Stroke Unit and Pediatric Neurology Department, Assistance publique-Hôpitaux de Paris, Paris-Saclay University, Hôpital Bicêtre, le Kremlin-Bicêtre, France.; Rolland A; Neurology Department, Nantes University, CHU de Nantes, Nantes, France.; Bourcier R; Pediatric Department, Nantes University, CHU de Nantes, Nantes, France.; Triquenot-Bagan A; Neurology Department, Rouen University, CHU de Rouen, Rouen, France.; Marnat G; Neuroradiology Department, Bordeaux University, CHU de Bordeaux, Bordeaux, France.; Neau JP; Neurology Department. Poiters University, CHU de Poitiers, Poitiers, France.; Joriot S; Pediatric Neurology Department, Lille University, CHU de Lille, Lille, France.; Perez A; Pediatric Department, Strasbourg University, CHU de Strasbourg, Strasbourg, France.; Guillen M; Neurology Department, Rennes University, CHU de Rennes, Rennes, France.; Perivier M; Pediatric Department, Tours University, CHU de Tours, Tours, France.; Audic F; Pediatric Neurology Department, Aix-Marseille University, CHU la Timone, Marseille, France.; Hak JF; Neuroradiology, Aix-Marseille University, CHU la Timone, Marseille, France.; Denier C; Pediatric Stroke Unit and Pediatric Neurology Department, Assistance publique-Hôpitaux de Paris, Paris-Saclay University, Hôpital Bicêtre, le Kremlin-Bicêtre, France.; Naggara O; Assistance publique-Hôpitaux de Paris, French Center for Pediatric Stroke, France.; Pediatric Neurology Department, Assistance publique-Hôpitaux de Paris, Inserm, Hôpital Necker-Enfants malades, Paris, France.; GHU Paris Psychiatrie et Neurosciences, CH Sainte-Anne, Inserm, Université de Paris Cité, Institut de psychiatrie et neurosciences de Paris, Service d'imagerie morphologique et fonctionnelle, UMRS1266, Paris, France.

Publisher: American Medical Association Country of Publication: United States NLM ID: 101729235 Publication Model: Electronic Cited Medium: Internet ISSN: 2574-3805 (Electronic) Linking ISSN: 25743805 NLM ISO Abbreviation: JAMA Netw Open Subsets: MEDLINE

Engel, Camille; Valence, Stephanie; Delplancq, Geoffroy; Maroofian, Reza; Kuentz, Paul; Cabrol, Christelle; Brischoux-Boucher, Elise; Salpietro, Vincenzo; Villard, Laurent; Doco-Fenzy, Martine; Odent, Sylvie; Morris-Rosendahl, Deborah; Zaki, Maha; Gerard, Marion; Brusco, Alfredo; Putoux, Audrey; Poulton, Cathryn; Coubes, Christine; Mignot, Cyril; Bubshait, Dalal; Kraus, Dror; Alkuraya, Fowzan; Scheffer, Ingrid; Engels, Hartmut; Wagner, Johanna; Gleeson, Joseph; Kutsche, Kerstin; Massingham, Laure; Pasquier, Laurent; Penney, Lynette; Cilio, Maria Roberta; Cornet, Marie-Coralie; Di Giacomo, Marilena Carmela; Rio, Marlene; Wagner, Matias; Striano, Pasquale; Straussberg, Rachel; Kaiyrzhanov, Rauan; Srivastava, Siddarth; Baglioni, Valentina; Vitobello, Antonio; Rougeot, Christelle; Valente, Enza Maria; Houlden, Henry; Goffeney, Joanna; Bruel, Ange-Line; Schneider, Amy; Vanmaldergem, Lionel; Burglen, Lydie; Piard, Juliette

EUROPEAN JOURNAL OF HUMAN GENETICS; MAY 11 2023, 31 p458-p459, 2p. Supplement: 1

Henderson NB; Butler BV; Goffeney B

Publisher: Wiley Country of Publication: United States NLM ID: 0217132 Publication Model: Print Cited Medium: Print ISSN: 0021-9762 (Print) Linking ISSN: 00219762 NLM ISO Abbreviation: J Clin Psychol Subsets: MEDLINE