부산대학교 도서관

C. Choquel; E. Geslin; E. Metzger; B. Jesus; A. Prins; E. Houliez; M. Schweizer; T. Jauffrais; É. Bénéteau; A. Mouret

Journal of Micropalaeontology, Vol 45, Pp 51-72 (2026)

Olivier Maillard; David Hirschinger; Samuel Bénéteau; Yatrika Koumar; Adrien Vague; Rémi Girerd; Laura DiAscia; Julien Jabot; Julien Cousty; Andry Randrianjohany; Antoine Bertolotti; Loïc Raffray

PLoS ONE, Vol 18, Iss 5, p e0285900 (2023)

Marlhand C Hemilembolo; Jérémy T Campillo; Valentin Dupasquier; Elodie Lebredonchel; Samuel Beneteau; Ludovic G Rancé; Glorifié Madoulou Moulabou; Ange Clauvel Niama; Richard R Bileckot; Sébastien D S Pion; Michel Boussinesq; François Missamou; Cédric B Chesnais

PLoS Neglected Tropical Diseases, Vol 19, Iss 9, p e0013491 (2025)

Dorion, C.; Blondy, P.; Madrangeas, V.; Zahr, A. H.; Zhang, L. Y.; Ghalem, A.; Beneteau, A.; Rabanne, M.; Stefanini, R.

2019 49th European Microwave Conference (EuMC) European Microwave Conference (EuMC), 2019 49th. :176-179 Oct, 2019

B.F. Melingui; E. Leroy-Terquem; J.V. Taguebue; T.C. Eap; L. Borand; C. Khosa; R. Moh; J. Mwanga-Amumpaire; S. Beneteau; M.T. Eang; I. Manhiça; A. Mustapha; O. Marcy; E. Wobudeya; P.Y. Norval; M. Bonnet; on behalf of the TB-Speed study group

IJTLD Open, Vol 1, Iss 10, Pp 449-455 (2024)

Zahr, A.H.; Zhang, L.Y.; Dorion, C.; Deveautour, A.; Beneteau, A.; Stefanini, R.; Blondy, P.

2019 European Microwave Conference in Central Europe (EuMCE) European Microwave Conference in Central Europe (EuMCE), 2019. :336-338 May, 2019

Zahr, A.H.; Zhang, L.Y.; Dorion, C.; Deveautour, A.; Beneteau, A.; Stefanini, R.; Blondy, P.; Courtade, F.; Kiryukhina, K.; Pressecq, F.

2018 Symposium on Design, Test, Integration & Packaging of MEMS and MOEMS (DTIP) Design, Test, Integration & Packaging of MEMS and MOEMS (DTIP), 2018 Symposium on. :1-4 May, 2018

B. F. Melingui; E. Leroy-Terquem; M. Palmer; J-V. Taguebue; A. P. Wachinou; J. Gaudelus; A. Salomao; D. Bunnet; T. C. Eap; L. Borand; C. Chabala; C. Khosa; R. Moh; J. Mwanga-Amumpere; M. T. Eang; I. Manhiça; A. Mustapha; S. Beneteau; L. Falzon; J. A. Seddon; L. Berteloot; E. Wobudeya; O. Marcy; M. Bonnet; P. Y. Norval

IJTLD Open, Vol 1, Iss 2, Pp 76-82 (2024)

Deb, W. ; Joubert, M. ; Cogné, B. ; Vincent, M. ; Ghesh, L. ; Bézieau, S. ; Le Vaillant, C. ; Beneteau, C.

In European Journal of Medical Genetics July 2023 66(7)

Domenach L; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, F-33000, France. louis.domenach@chu-bordeaux.fr.; Rooryck C; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, F-33000, France.; Univ. Bordeaux, Génétique et Métabolisme (MRGM), INSERM U1211, Bordeaux, F-33000, France.; Legendre M; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, F-33000, France.; Bouchghoul H; Service de Gynécologie Obstétrique, CHU de Bordeaux, Bordeaux, F-33000, France.; Beneteau C; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, F-33000, France.; Margot H; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, F-33000, France. henri.margot@hug.ch.

Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794 (Electronic) Linking ISSN: 17558794 NLM ISO Abbreviation: BMC Med Genomics Subsets: MEDLINE

Dafsari HS; Department of Pediatrics and Center for Rare Diseases, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.; Max Planck Institute for Biology of Aging and Cologne Excellence Cluster for Aging-associated Diseases, Cologne, Germany.; Department of Pediatric Neurology, Evelina London Children's Hospital, Guy's & St Thomas NHS Foundation Trust, London, UK.; Randall Center for Cell and Molecular Biophysics, Muscle Signaling Section, Faculty of Life Sciences and Medicine (FoLSM), King's College London, London, UK.; Deneubourg C; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.; Singh K; UCL Consortium for Mitochondrial Research and Department of Cell and Developmental Biology, University College London, London, UK.; Maroofian R; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.; Suprenant Z; Vici Syndrome Foundation, Inc, Silver Spring, Maryland, USA.; Kho AL; Randall Center for Cell and Molecular Biophysics, Muscle Signaling Section, Faculty of Life Sciences and Medicine (FoLSM), King's College London, London, UK.; Ingham NJ; Wolfson Sensory Pain and Regeneration Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.; Steel KP; Wolfson Sensory Pain and Regeneration Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.; Sheshadri P; UCL Consortium for Mitochondrial Research and Department of Cell and Developmental Biology, University College London, London, UK.; Baur F; Department of Pediatrics and Center for Rare Diseases, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.; Max Planck Institute for Biology of Aging and Cologne Excellence Cluster for Aging-associated Diseases, Cologne, Germany.; Hentrich L; Department of Pediatrics and Center for Rare Diseases, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.; Max Planck Institute for Biology of Aging and Cologne Excellence Cluster for Aging-associated Diseases, Cologne, Germany.; Gerisch B; Max Planck Institute for Biology of Aging and Cologne Excellence Cluster for Aging-associated Diseases, Cologne, Germany.; Zamani M; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.; Department of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.; Alves C; Department of Radiology, Boston Children's Hospital, Boston, MA, USA.; Siddiqui A; Department of Radiology, Guy's and Saint Thomas' Hospitals NHS Trust, London, UK.; Dafsari HS; Department of Neurology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.; Salari M; Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Lang AE; Edmond J Safra Program in Parkinson's Disease, Krembil Brain Institute, University Health Network and the Department of Medicine, University of Toronto, Toronto, ON, Canada.; Harris M; Vici Syndrome Foundation, Inc, Silver Spring, Maryland, USA.; Abdelaleem A; Department of Neurology, Weill Cornell Medicine Qatar, Education City, Doha, Qatar.; Medical Molecular Genetics, Institute Human Genetics and Genome Research, National Research Centre, Dokki, Egypt.; Sadeghian S; Department of Neurology, University of Minnesota, Minneapolis, Minnesota, USA.; Azizimalamiri R; Department of Neurology, University of Minnesota, Minneapolis, Minnesota, USA.; Galehdari H; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.; Shariati G; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.; Department of Medical Genetics, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.; Sedaghat A; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.; Diabetes Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.; Zeighami J; Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Calame D; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Marafi D; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Duan R; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Boehnke A; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Clark GD; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Baylor Genetics Laboratories, Houston, TX, USA.; Mohila CA; Department of Pathology, Department of Pathology and Immunology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.; Steel D; Developmental Neurosciences, Zayed Centre for Research into Rare Disease in Children, UCL GOS-Institute of Child Health, London, UK.; Chopra S; Indraprastha Apollo Hospital, New Delhi, India.; Sharma S; Department of Pediatrics, Lady Hardinge Medical College and Associated Kalawati Saran Children's Hospital, New Delhi, India.; Kohlschmidt N; Institute for Clinical Genetics and Tumour Genetics, Bonn, Germany.; Laboratoire national de santé, National Center of Genetics, Dudelange, Luxembourg.; Patzer S; Department of Pediatrics, Krankenhaus St. Elisabeth und St. Barbara, Halle (Saale), Germany.; Saffari A; Division of Child Neurology and Metabolic Medicine, Department of Pediatrics I, Center for Pediatrics and Adolescent Medicine, Medical Faculty Heidelberg, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.; Ebrahimi-Fakhari D; Movement Disorders Program, Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.; Çavdartepe BE; Department of Medical Genetics, Konya City Hospital, Konya, Turkey.; Chang IJ; Department of Pediatrics, Division of Medical Genetics, University of California at San Francisco, San Francisco, CA, USA.; Beckman E; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA, USA.; Peters R; Christliches Kinderhospital Osnabrück, Osnabrück, Germany.; Fennell AP; Monash Genetics, Monash Health, Melbourne, Vic, Australia.; Department of Paediatrics, Monash University, Melbourne, Vic, Australia.; Lo B; Research Branch, Sidra Medicine, Doha; College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.; Averdunk L; Department of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.; Distelmaier F; Department of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.; Baethmann M; Department of Pediatrics, Hospital Dritter Orden, Munich, Germany.; Elmslie F; St George's University Hospitals NHS Foundation Trust, London, UK.; Joost K; Faculty of Medicine, University of Tartu, Tartu, Estonia.; Nampoothiri S; Department of Pediatric Genetics, Amrita Institute of Medical Sciences & Research Center, Cochin, India.; Yesodharan D; Department of Metabolic and Genetic Disorders, Ziv, Medical Center, Safed, Israel.; Mandel H; Department of Metabolic and Genetic Disorders, Ziv, Medical Center, Safed, Israel.; Kimball A; Harvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, MD, USA.; Kline AD; Harvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, MD, USA.; Mignot C; APHP, Hôpital Pitié-Salpêtrière, Département de Génétique, Centre de Reference Déficience Intellectuelle de Causes Rares, GRC UPMC Déficience Intellectuelle et Autisme, Paris, France.; Keren B; APHP, Hôpital Pitié-Salpêtrière, Département de Génétique, Centre de Reference Déficience Intellectuelle de Causes Rares, GRC UPMC Déficience Intellectuelle et Autisme, Paris, France.; Laugel V; Service de Pédiatrie, Centre Hospitalier Universitaire (CHU) de Strasbourg-Hautepierre, Strasbourg, France.; Õunap K; Department of Clinical Genetics, Genetics and Personalized Medicine Clinic, Tartu University Hospital and Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.; Devadathan K; Department of Pediatric Neurology, Government Medical College, Thiruvananthapuram, India.; van Berkestijn FMC; Department of Pediatric Neurology, University Medical Center Utrecht, Utrecht, the Netherlands.; Silwal A; St Bart's Health NHS Trust, London, UK.; Koene S; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.; Verma S; Children's Healthcare of Atlanta, Emory University, Atlanta, GA, USA.; Karim MY; Department of Pathology, Sidra Medicine, College of Medicine, Qatar University, Doha, Qatar.; Boubidi C; Department of Pediatrics A, Hussein Dey University Hospital Center, University of Algiers 1, Algiers, Algeria.; Aziz M; Department of Pediatric Neurology, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.; ElGhazali G; Department of Medical Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.; Mattas L; Stanford Children's Hospital, Palo Alto, CA, USA.; Miryounesi M; Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Hashemi-Gorji F; Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.; Alavi S; Palindrome, Isfahan, Iran.; Nouri N; Karyogen Lab, Isfahan, Iran.; Noruzinia M; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.; Kavousi S; Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.; Kamath A; Cardiff and Vale UHB-AWMGS, Cardiff, UK.; Jayawant S; Oxford University Hospitals NHS Foundation Trust, Oxford, UK.; Saneto R; Neuroscience Institute, Center for Integrated Brain Research, Department of Neurology/Division of Pediatric Neurology, Seattle Children's Hospital, Seattle, WA, USA.; Haridy NA; Department of Neurology, Faculty of Medicine, Assiut University, Assiut, Egypt.; Kart PO; Department of Pediatrics Neurology, Karadeniz Technical University, Trabzon, Turkey.; Cansu A; Genetics Department, Nantes University Hospital, Nantes, France.; Joubert M; Genetics Department, Nantes University Hospital, Nantes, France.; Beneteau C; Genetics Department, Nantes University Hospital, Nantes, France.; Stuurman KE; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.; Wilke M; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.; Barakat TS; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.; Tajsharghi H; School of Health Science, Division Biomedicine and Translational Medicine, University of Skovde, Skovde, Sweden.; Scardamaglia A; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.; Vallian S; Department of Cell and Molecular Biology & Microbiology, Faculty of Science and Technology, University of Isfahan, Isfahan, Iran.; Hız S; Faculty of Medicine, Pediatric Neurology Department, Dokuz Eylül University, Izmir, Turkey.; Shoeibi A; Department of Neurology, Mashhad University of Medical Sciences, Mashhad, Iran.; Boostani R; Department of Neurology, Mashhad University of Medical Sciences, Mashhad, Iran.; Hashemi N; Department of Pediatrics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.; Rare Pediatric Neurological Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.; Babaei M; Department of Pediatrics, North Khorasan University of Medical Sciences, Bojnurd, Iran.; Alsaleh NS; Department of Genetics and Precision Medicine, King Abdullah Specialized Children's Hospital, King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.; Porter J; Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, UT, USA.; Attié-Bitach T; Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Paris, France.; Marzin P; Service de Médecine Génomique des Maladies Rares, Hôpital Necker-Enfants Malades, Paris, France.; Wicher D; Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland.; Gold JI; Division of Medical Genetics, Department of Pediatrics, Cohen Children's Medical Center, New Hyde Park, NY, USA.; Schuler E; Division of Child Neurology and Metabolic Medicine, Department of Pediatrics I, Center for Pediatrics and Adolescent Medicine, Medical Faculty Heidelberg, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.; Kashgari A; Department of Clinical Genetics and Precision Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; Alanazi RF; Department of Clinical Genetics and Precision Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; Eyaid W; Department of Clinical Genetics and Precision Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.; Engelen M; Amsterdam Leukodystrophy Center, Department of Pediatric Neurology, Emma Children's Hospital, and Amsterdam Neuroscience, Cellular & Molecular Mechanisms, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, the Netherlands.; Langeveld M; Department of Endocrinology and Metabolism, Amsterdam UMC, Research Institute Gastroenterology, Endocrinology & Metabolism (AGEM), University of Amsterdam, Amsterdam, the Netherlands.; Stüve B; Department for Neuropediatrics, DRK Children's Hospital Siegen, Siegen, Germany.; Li Y; Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany.; Yigit G; Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany.; DZHK (German Center for Cardiovascular Research), Partner Site Lower Saxony, Göttingen, Germany.; Wollnik B; Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany.; DZHK (German Center for Cardiovascular Research), Partner Site Lower Saxony, Göttingen, Germany.; Cluster of Excellence 'Multiscale Bioimaging: From Molecular Machines To Networks of Excitable Cells' (MBExC), University of Göttingen; German Center for Child and Adolescent Health (DZKJ), Partner Site Göttingen, Göttingen, Germany.; Monje MHG; Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.; Krainc D; Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.; Mencacci NE; Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.; Bakhtiari S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.; Kruer M; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.; Argilli E; Department of Neurology, University of California San Francisco Division of Hospital Medicine, San Francisco, CA, USA.; Sherr E; Department of Neurology, University of California San Francisco Division of Hospital Medicine, San Francisco, CA, USA.; Jamshidi Y; Molecular and Clinical Sciences Institute, St. George's University of London, London, UK.; Karimiani EG; Molecular and Clinical Sciences Institute, St. George's University of London, London, UK.; Cheung YWS; Life Sciences Institute, Department of Biochemistry and Molecular Biology, The University of British Columbia, Vancouver, BC, Canada.; Karin I; Friedrich-Baur-Institute, Department of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität München, Munich, Germany.; Zifarelli G; CENTOGENE GmbH, Rostock, Germany.; Bauer P; CENTOGENE GmbH, Rostock, Germany.; Chung WK; Department of Pediatrics, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.; Lupski JR; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Kurian MA; Developmental Neurosciences, Zayed Centre for Research into Rare Disease in Children, UCL GOS-Institute of Child Health, London, UK.; Dötsch J; Department of Pediatrics and Center for Rare Diseases, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.; von Kleist-Retzow JC; Department of Pediatrics and Center for Rare Diseases, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.; Klopstock T; Friedrich-Baur-Institute, Department of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität München, Munich, Germany.; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.; Wagner M; Institute of Human Genetics, School of Medicine and Health, Technische Universität München, Munich, Germany.; Yip C; Life Sciences Institute, Department of Biochemistry and Molecular Biology, The University of British Columbia, Vancouver, BC, Canada.; Roos A; Department of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- and Behavioral Sciences, University Duisburg-Essen, Essen, Germany.; Department of Neurology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University, Düsseldorf, Germany.; Brain and Mind Research Institute, Children's Hospital of Eastern Ontario Research Institute, Ottawa, ON, Canada.; Carsetti R; Immunology Research Area, B Cell Unit, Ospedale Pediatrico Bambino Gesù IRCCS, Rome, Italy.; Dionisi-Vici C; Division of Metabolic Diseases and Hepatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Gautel M; Randall Center for Cell and Molecular Biophysics, Muscle Signaling Section, Faculty of Life Sciences and Medicine (FoLSM), King's College London, London, UK.; Duchen MR; UCL Consortium for Mitochondrial Research and Department of Cell and Developmental Biology, University College London, London, UK.; Antebi A; Max Planck Institute for Biology of Aging and Cologne Excellence Cluster for Aging-associated Diseases, Cologne, Germany.; Houlden H; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.; Fanto M; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.; Jungbluth H; Department of Pediatric Neurology, Evelina London Children's Hospital, Guy's & St Thomas NHS Foundation Trust, London, UK.; Randall Center for Cell and Molecular Biophysics, Muscle Signaling Section, Faculty of Life Sciences and Medicine (FoLSM), King's College London, London, UK.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7707449 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8249 (Electronic) Linking ISSN: 03645134 NLM ISO Abbreviation: Ann Neurol Subsets: MEDLINE

Vegas N; General Pediatrics Unit, Necker University Hospital, Assistance Publique-Hôpitaux de Paris, 149 rue de Sèvres, 75015, Paris, France. nancy.vegas@aphp.fr.; Malformation and Embryology Laboratory, IMAGINE Institute, Paris, France. nancy.vegas@aphp.fr.; Université Paris Cité, Paris, France. nancy.vegas@aphp.fr.; Reference Centre for Rare Diseases Centre de Référence Maladies Rares « Syndromes de Pierre Robin et troubles de succion-déglutition congénitaux », Necker University Hospital, Paris, France. nancy.vegas@aphp.fr.; Rio M; Medical Genetics Department, Necker University Hospital, Paris, France.; Adnot P; General Pediatrics Unit, Necker University Hospital, Assistance Publique-Hôpitaux de Paris, 149 rue de Sèvres, 75015, Paris, France.; Université Paris Cité, Paris, France.; Reference Centre for Rare Diseases Centre de Référence Maladies Rares « Syndromes de Pierre Robin et troubles de succion-déglutition congénitaux », Necker University Hospital, Paris, France.; Soupre V; Reference Centre for Rare Diseases Centre de Référence Maladies Rares « Syndromes de Pierre Robin et troubles de succion-déglutition congénitaux », Necker University Hospital, Paris, France.; Maxillo-Facial and Plastic Surgery Unit, Necker University Hospital, Paris, France.; Petit F; Clinique de Génétique Guy Fontaine, CHU Lille, Hôpital Jeanne de Flandre, Lille, France.; Ghoumid J; Clinique de Génétique Guy Fontaine, CHU Lille, Hôpital Jeanne de Flandre, Lille, France.; Toutain A; Service de Génétique, CHRU de Tours, Hôpital Bretonneau, Tours, France.; Dieterich K; Unité de Génétique Clinique, CHU Grenoble, Hôpital Couple-Enfant, Grenoble, France.; Marey I; Unité de Génétique Clinique, CHU Grenoble, Hôpital Couple-Enfant, Grenoble, France.; Gilbert-Dussardier B; Service de Génétique Médicale, CHU de Poitiers, Poitiers, France.; Le Guyader G; Service de Génétique Médicale, CHU de Poitiers, Poitiers, France.; Francannet C; Service de Génétique Médicale, CHU de Clermont-Ferrand, Hôpital d'Estaing, Clermont-Ferrand, France.; Schaefer E; Service de Génétique Médicale, CHU de Strasbourg, Hôpital de Hautepierre, Strasbourg, France.; Perrin L; Unité de Génétique Clinique, CHU Paris, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris, France.; Nizon M; Unité de Génétique Clinique, CHU de Nantes, Nantes, France.; Beneteau C; Unité de Génétique Clinique, CHU de Nantes, Nantes, France.; Genevieve D; Département de Génétique Médicale, CHU de Montpellier, Hôpital Arnaud de Villeneuve, Montpellier, France.; Willems M; Département de Génétique Médicale, CHU de Montpellier, Hôpital Arnaud de Villeneuve, Montpellier, France.; Faivre L; Centre de Génétique, Hôpital d'enfants, CHU Dijon Bourgogne, Hôpital François Mitterand, Dijon, France.; Grimaldi M; Centre de Génétique, Hôpital d'enfants, CHU Dijon Bourgogne, Hôpital François Mitterand, Dijon, France.; Melki J; Unité de Génétique Médicale - Médecine néonatale, Centre Hospitalier Sud Francilien and INSERM, UMR-1195, Le Kremlin-Bicêtre, France.; Stoeva R; Laboratoire de Génétique Médicale et Cytogénétique, Centre Hospitalier Le Mans, Le Mans, France.; Putoux A; Service de Génétique, CHU de Lyon, GH Est-Hôpital Femme Mère Enfant, Lyon, France.; Pons L; Laboratoire de Biologie Médicale, Unité Fonctionnelle de Cytogénétique, Centre Hospitalier de Valence, Valence, France.; Benistan K; Service de Génétique, Hôpital Raymond Poincaré, Assistance Publique-Hôpitaux de Paris, Garches, France.; Amiel J; Malformation and Embryology Laboratory, IMAGINE Institute, Paris, France.; Université Paris Cité, Paris, France.; Medical Genetics Department, Necker University Hospital, Paris, France.; Abadie V; General Pediatrics Unit, Necker University Hospital, Assistance Publique-Hôpitaux de Paris, 149 rue de Sèvres, 75015, Paris, France.; Université Paris Cité, Paris, France.; Reference Centre for Rare Diseases Centre de Référence Maladies Rares « Syndromes de Pierre Robin et troubles de succion-déglutition congénitaux », Necker University Hospital, Paris, France.

Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE

Vermesan, O.; Blystad, L.-C.; Bahr, R.; Hjelstuen, M.; Beneteau, L.; Froelich, B.

Proceedings of the 31st European Solid-State Circuits Conference, 2005. ESSCIRC 2005. Solid-State Circuits Conference Solid-State Circuits Conference, 2005. ESSCIRC 2005. Proceedings of the 31st European. :287-290 2005

Palmcrantz, S; Zampakas, A; Kullander, K; Mårdby, A-C; Ahl, M; Beneteau, M; Cars, T; Borg, J

TOXICON. 271:108833-108833

Möller B; Department of Pediatrics, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Becker LL; Department of Pediatric Neurology, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.; Center for Chronically Sick Children, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.; Institute for Cell Biology and Neurobiology, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.; Saffari A; Heidelberg University, Medical Faculty Heidelberg, University Hospital Heidelberg, Center for Pediatrics and Adolescent Medicine, Department of Pediatrics I, Division of Child Neurology and Metabolic Medicine, 69120 Heidelberg, Germany.; Afenjar A; Reference Center for Malformations and Congenital Diseases of the Cerebellum and Intellectual Disabilities of Rare Causes, Department of Genetics and Medical Embryology, Sorbonne University, Trousseau Hospital Paris, 75012 Paris, France.; Coci EG; Department of Paediatrics, Otto-von-Guericke-University Magdeburg, 39120 Magdeburg, Germany.; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, 2100 Copenhagen, Denmark.; Williamson R; Akron Children's Hospital Genetic Center, Akron, OH 44308, USA.; Ward-Melver C; Akron Children's Hospital Genetic Center, Akron, OH 44308, USA.; Gibaud M; Service de pédiatrie, CHU de Nantes, 44000 Nantes, France.; Sedláčková L; Neurogenetic Laboratory, Department of Pediatric Neurology, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital, Full Member of the ERN EpiCARE, 150 06 Prague, Czech Republic.; Laššuthová P; Neurogenetic Laboratory, Department of Pediatric Neurology, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital, Full Member of the ERN EpiCARE, 150 06 Prague, Czech Republic.; Libá Z; Department of Pediatric Neurology, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital, Full Member of the ERN EpiCARE, 150 06 Prague, Czech Republic.; Vlčková M; Department of Biology and Medical Genetics, Second Faculty of Medicine, Charles University in Prague and Motol University Hospital, Full Member of the ERN EpiCARE, 150 06 Prague, Czech Republic.; William N; Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55901, USA.; Klee EW; Departments of Clinical Genomics and Neurology, Mayo Clinic, Rochester, MN 55905, USA.; Gavrilova RH; Departments of Clinical Genomics and Neurology, Mayo Clinic, Rochester, MN 55905, USA.; Lévy J; Genetics Department, AP-HP, Robert-Debré University Hospital, 75019 Paris, France.; Capri Y; Genetics Department, AP-HP, Robert-Debré University Hospital, 75019 Paris, France.; Scavina M; Division of Neurology, Nemours Children's Health, Wilmington, Delaware 19803, USA.; Körner RW; Department of Pediatrics, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Valivullah Z; Center for Mendelian Genomics, Broad Institute Harvard, Cambridge, MA 02142, USA.; Weiß C; Department of Pediatric Neurology, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.; Center for Chronically Sick Children, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.; Möller GM; Berlin University of Applied Sciences and Technology, 10587 Berlin, Germany.; Frazier Z; Department of Neurology, Rosamund Stone Zander Translational Neuroscience Center, Boston Children's Hospital, Boston, MA 02115, USA.; Roberts A; Center for Cardiovascular Genetics, Boston Children's Hospital, Boston, MA 02115, USA.; Gener B; Department of Genetics, Cruces University Hospital, Biobizkaia Health Research Institute, Barakaldo 48903, Spain.; Scala M; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 16147 Genoa, Italy.; U.O.C. Genetica Medica, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.; Striano P; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 16147 Genoa, Italy.; Pediatric Neurology and Muscular Diseases Unit, IRCCS Giannina Gaslini Institute, 16147 Genoa, Italy.; Zara F; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 16147 Genoa, Italy.; U.O.C. Genetica Medica, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy.; Thiel M; Department of Pediatrics, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Sinnema M; Department of Clinical Genetics, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.; Kamsteeg EJ; Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.; Donkervoort S; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke Neurogenetics Branch, National Institutes of Health, Bethesda, MD 20892, USA.; Duboc V; Department of Medical Genetics, Université Côte D'Azur, Centre Hospitalier Universitaire Nice, 06000 Nice, France.; Zaafrane-Khachnaoui K; Department of Medical Genetics, Université Côte D'Azur, Centre Hospitalier Universitaire Nice, 06000 Nice, France.; Elkhateeb N; Department of Clinical Genetics, Cambridge University Hospitals NHS Trust, Cambridge CB2 3EH, UK.; Department of Pediatrics, Pediatric Neurology and Metabolic Medicine unit, Kasr Al-Ainy School of Medicine, Cairo University, 4390330 Cairo, Egypt.; Selim L; Department of Pediatrics, Pediatric Neurology and Metabolic Medicine unit, Kasr Al-Ainy School of Medicine, Cairo University, 4390330 Cairo, Egypt.; Margot H; Department of Medical Genetics, University Hospital of Bordeaux, 33076 Bordeaux, France.; Marin V; Department of Medical Genetics, University Hospital of Bordeaux, 33076 Bordeaux, France.; Beneteau C; Department of Medical Genetics, University Hospital of Bordeaux, 33076 Bordeaux, France.; Isidor B; Genetics Department, Nantes University, CHU de Nantes, 44000 Nantes, France.; Cogne B; Genetics Department, Nantes University, CHU de Nantes, 44000 Nantes, France.; Keren B; Genetic Department, Pitié-Salpêtrière Hospital, AP-HP, Sorbonne University, 75013 Paris, France.; Küsters B; Department of Pathology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.; Beggs AH; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, MA 02445, USA.; Sveden A; Department of Neurology, Rosamund Stone Zander Translational Neuroscience Center, Boston Children's Hospital, Boston, MA 02115, USA.; Chopra M; Department of Neurology, Rosamund Stone Zander Translational Neuroscience Center, Boston Children's Hospital, Boston, MA 02115, USA.; Genetti CA; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, MA 02445, USA.; Nicolai J; Department of Neurology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.; Dötsch J; Department of Pediatrics, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Center for Rare Diseases, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Koy A; Department of Pediatrics, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Center for Rare Diseases, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Bönnemann CG; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke Neurogenetics Branch, National Institutes of Health, Bethesda, MD 20892, USA.; von der Hagen M; Department of Neuropediatrics, Medical Faculty Carl Gustav Carus, Technische Universität Dresden, 01307  Dresden, Germany.; von Kleist-Retzow JC; Department of Pediatrics, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Center for Rare Diseases, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Voermans NC; The Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, 6525 Nijmegen, The Netherlands.; Jungbluth H; Department of Paediatric Neurology-Neuromuscular Service, Evelina Children's Hospital, Guy's & St Thomas' NHS Foundation Trust, London SE1 7EH, UK.; Randall Centre for Cell and Molecular Biophysics, Muscle Signalling Section, Faculty of Life Sciences and Medicine (FoLSM), King's College London, London SE1 1YR, UK.; Dafsari HS; Department of Pediatrics, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Center for Rare Diseases, Faculty of Medicine, University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.; Department of Paediatric Neurology-Neuromuscular Service, Evelina Children's Hospital, Guy's & St Thomas' NHS Foundation Trust, London SE1 7EH, UK.; Randall Centre for Cell and Molecular Biophysics, Muscle Signalling Section, Faculty of Life Sciences and Medicine (FoLSM), King's College London, London SE1 1YR, UK.; Max-Planck-Institute for Biology of Ageing, 50931 Cologne, Germany.; Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (CECAD), 50931 Cologne, Germany.

Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

Sauvestre C; CHU Bordeaux, Service de Génétique Médicale (C.S., A.B., C. Beneteau, V.M., C.R.).; Bouchatal A; CHU Bordeaux, Service de Génétique Médicale (C.S., A.B., C. Beneteau, V.M., C.R.).; Beneteau C; CHU Bordeaux, Service de Génétique Médicale (C.S., A.B., C. Beneteau, V.M., C.R.).; Michaud V; CHU Bordeaux, Service de Génétique Médicale (C.S., A.B., C. Beneteau, V.M., C.R.).; Univ. Bordeaux, Maladies Rares: Génétique et Métabolisme (MRGM), INSERM U1211 (V.M., C.R.).; Blanc P; Laboratoire SeqOIA-PFMG2025, Paris (P. Blanc).; Bouvagnet P; Centre de Diagnostic Prénatal, Hôpital MFME, Fort de France, Martinique, France (P. Bouvagnet).; Chung WK; Department of Pediatrics, Boston Children's Hospital & Harvard Medical School, MA (W.K.C.).; Marcadier J; Department of Pediatrics (J.M., M.A.T.).; Thomas MA; Department of Pediatrics (J.M., M.A.T.).; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Alberta, Canada (M.A.T.).; Karstensen HG; Department of Genetics, Center of Diagnostics, Copenhagen University Hospital-Rigshospitalet, Denmark (H.G.K., A.P.B.).; Born AP; Department of Genetics, Center of Diagnostics, Copenhagen University Hospital-Rigshospitalet, Denmark (H.G.K., A.P.B.).; Breen C; Manchester Centre for Genomic Medicine, St Mary's Hospital (C. Breen).; Evolution, Infection & Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, United Kingdom (C. Breen).; Xiong S; Shanghai 1st Maternity & Infant Hospital, Tongji University, China (S.X.).; Ades LC; Department of Clinical Genetics, Children's Hospital at Westmead, Sydney Children's Hospital Network, NSW, Australia (L.C.A.).; Dixit A; Nottingham Univ Hospitals, United Kingdom (A.D.).; Fradin M; Service de Génétique Médicale, CLAD Ouest, CHU de Rennes, France (M.F.).; Rooryck C; CHU Bordeaux, Service de Génétique Médicale (C.S., A.B., C. Beneteau, V.M., C.R.).; Univ. Bordeaux, Maladies Rares: Génétique et Métabolisme (MRGM), INSERM U1211 (V.M., C.R.).

Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101714113 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2574-8300 (Electronic) Linking ISSN: 25748300 NLM ISO Abbreviation: Circ Genom Precis Med Subsets: MEDLINE; In Process

Abanov, Ar.; Beneteau, C.; Khavinson, D.; Teodorescu, R.

Journal d'Analyse Mathematique, Volume 139, pp. 677-696, (2019)

Palmer, E.; Pusch, M.; Picollo, A.; Forwood, C.; Nguyen, M.; Suckow, V.; Gibbons, J.; https://orcid.org/0000-0003-4747-322X; Hoff, A.; Sigfrid, L.; Megarbane, A.; Nizon, M.; Cogné, B.; Beneteau, C.; Alkuraya, F.; Chedrawi, A.; Hashem, M.; Stamberger, H.; Weckhuysen, S.; Vanlander, A.; Ceulemans, B.; Rajagopalan, S.; Nunn, K.; Arpin, S.; Raynaud, M.; Motter, C.; Ward-Melver, C.; Janssens, K.; Meuwissen, M.; Beysen, D.; Kalscheuer, V.; https://orcid.org/0000-0001-6898-3259

Molecular Psychiatry

Margot H; Univ. Bordeaux, MRGM INSERM U1211, CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, France.; Pizano A; Aquitaine Autism Resources Centre, Centre Hospitalier Charles-Perrens, University Pole of Child and Adolescent Psychiatry, Bordeaux, France.; Amestoy A; Aquitaine Autism Resources Centre, Centre Hospitalier Charles-Perrens, University Pole of Child and Adolescent Psychiatry, Bordeaux, France.; Lacombe D; Univ. Bordeaux, MRGM INSERM U1211, CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, France.; Berges C; Univ. Bordeaux, MRGM INSERM U1211, CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, France.; Beneteau C; Univ. Bordeaux, MRGM INSERM U1211, CHU de Bordeaux, Service de Génétique Médicale, Bordeaux, France.; Innes AM; Department of Medical Genetics and Pediatrics and Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Canada.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235745 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4876 (Electronic) Linking ISSN: 15524868 NLM ISO Abbreviation: Am J Med Genet C Semin Med Genet Subsets: MEDLINE

Favier M; Centre de Génétique Humaine, Centre Hospitalier Universitaire de Besançon, Université de Franche-Comté, Besançon, France.; SoFFoet - Société Française de Foetopathologie, Paris, France.; Brischoux-Boucher E; Centre de Génétique Humaine, Centre Hospitalier Universitaire de Besançon, Université de Franche-Comté, Besançon, France.; Pyle LC; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Mottet N; Département d'Obstétrique et de Gynécologie, Centre Hospitalier Universitaire de Besançon, Université de Bourgogne Franche-Comté, Besançon, France.; Auber-Lenoir M; Département de Radiologie, Imagerie pédiatrique, prénatale et sénologie, Centre Hospitalier Universitaire de Besançon, Université de Bourgogne Franche-Comté, Besançon, France.; Cattin J; Département d'Obstétrique et de Gynécologie, Centre Hospitalier Universitaire de Besançon, Université de Bourgogne Franche-Comté, Besançon, France.; Dahlen E; Université de Franche-Comté, Centre Hospitalier Universitaire de Besançon, Oncobiologie Génétique Bioinformatique, FHU-TRANSLAD et Institut GIMI, Besançon, France.; Cabrol C; Centre de Génétique Humaine, Centre Hospitalier Universitaire de Besançon, Université de Franche-Comté, Besançon, France.; Arbez-Gindre F; Anatomie et cytologie pathologiques, Foetopathologie, Centre Hospitalier Universitaire de Besançon, Université de Bourgogne Franche-Comté, Besançon, France.; Attié-Bitach T; Laboratoire de biologie médicale multisites SeqOIA, Assistance Publique Hôpitaux de Paris, Paris, France.; Institut Imagine, INSERM U1163, Université Paris Descartes, Paris, France.; Boute O; Pôle de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille, Lille, France.; Devisme L; Pôle de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille, Lille, France.; Trost D; Génétique et Cytogénétique, Laboratoire Cerba, Saint-Ouen l'Aumône, Paris, France.; Boughalem A; Génétique et Cytogénétique, Laboratoire Cerba, Saint-Ouen l'Aumône, Paris, France.; Chitayat D; Mount Sinai Hospital, University of Toronto, Toronto, Canada.; Prasov L; Department of Ophthalmology and Visual Sciences, W.K. Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan, USA.; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA.; Chorin O; Institute of Rare Diseases, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hashomer, Israel.; Rein-Rothschild A; Institute of Rare Diseases, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hashomer, Israel.; School of Medicine, Faculty of Medical and Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.; Kassif E; School of Medicine, Faculty of Medical and Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.; Department of Obstetrics and Gynecology, Sheba Medical Center, Tel Hashomer, Israel.; Weissbach T; School of Medicine, Faculty of Medical and Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.; Department of Obstetrics and Gynecology, Sheba Medical Center, Tel Hashomer, Israel.; Hendon LG; Mississippi Medical Center, Jackson, Mississippi, USA.; Adam MP; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, Washington, USA.; Quelin C; SoFFoet - Société Française de Foetopathologie, Paris, France.; Service de génétique clinique, Centre Hospitalier Universitaire de Rennes, Université de Rennes, Rennes, France.; Jaillard S; Service de Cytogénétique et Biologie Cellulaire, Centre Hospitalier Universitaire de Rennes, Université de Rennes, Rennes, France.; Mary L; Service de Cytogénétique et Biologie Cellulaire, Centre Hospitalier Universitaire de Rennes, Université de Rennes, Rennes, France.; Aukema SM; Department of Medical Genetics, Carl von Ossietzky University, Oldenburg, Germany.; Heijligers M; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.; de Die-Smulders C; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.; Stegmann S; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.; Badalato L; Department of Pediatrics, Kingstone General Hospital, Queen's University, Kingston, Canada.; Ben-Yehuda A; Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel.; Beneteau C; SoFFoet - Société Française de Foetopathologie, Paris, France.; Service de Génétique Médicale, Centre Hospitalier Universitaire de Bordeaux, Université de Bordeaux, Bordeaux, France.; Forey PL; Département d'Obstétrique et de Gynécologie, Centre Hospitalier Universitaire de Grenoble, Université de Grenoble, Grenoble, France.; Kuentz P; Université de Franche-Comté, Centre Hospitalier Universitaire de Besançon, Oncobiologie Génétique Bioinformatique, FHU-TRANSLAD et Institut GIMI, Besançon, France.; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France.; Piard J; Centre de Génétique Humaine, Centre Hospitalier Universitaire de Besançon, Université de Franche-Comté, Besançon, France.; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France.

Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE