부산대학교 도서관

Soilly, AL; Robert-Viard, C; Besse, C; Bruel, AL; Gerard, B; Boland, A; Piton, A; Duffourd, Y; Muller, J; Poë, C; Jouan, T; El Doueiri, S; Faivre, L; Bacq-Daian, D; Isidor, B; Genevieve, D; Odent, S; Philip, N; Doco-Fenzy, M; Lacombe, D; Asensio, ML; Deleuze, JF; Binquet, C; Arpin, S; Blanchet, P; Blesson, S; Boute-Benejean, O; Busa, T; Colin, E; Coubes, C; Devillard, F; Edery, P; El Chehadeh, S; Fradin, M; Goldenberg, A; Guerrot, A-M; Herenger, Y; Houcinat, N; Jean-Marcais, N; Jouk, P. S.; Lambert, L; Lavillaureix, A; Legendre, M; Leheup, B; Manouvrier, S; Mercier, S; Moutton, S; Nizon, M; Pasquier, L; Petit, F; Pinson, L; Poirsier, C; Pons, L; Putoux, A; Quelin, C; Renaud, M; Rossi, M; Sorlin, A; Spodenkiewicz, M; Thevenon, J; Toutain, A; Van-Gils, J; Vanlerberghe, C; Verloes, A; Vincent, M; Vincent-Delorme, C; Willems, M; Ziegler, A

BMC Health Services Research. April 21, 2023, Vol. 23 Issue 1

Cabet S; Pediatric and Fetal Imaging Department, Femme-Mère-Enfant Hospital, Hospices Civils de Lyon, Claude Bernard Lyon 1 University, Lyon, France.; Institut NeuroMyoGène, CNRS UMR5292, INSERM U1028, Claude Bernard Lyon 1 University, Lyon, France.; Multidisciplinary Center for Prenatal Diagnosis, Femme-Mère-Enfant Hospital, Hospices Civils de Lyon, Claude Bernard Lyon 1 University, Lyon, France.; Putoux A; Multidisciplinary Center for Prenatal Diagnosis, Femme-Mère-Enfant Hospital, Hospices Civils de Lyon, Claude Bernard Lyon 1 University, Lyon, France.; Department of Genetics, Groupement Hospitalier Est, Hospices Civils de Lyon, Claude Bernard Lyon 1 University, Lyon, France.; Lesca G; Institut NeuroMyoGène, CNRS UMR5292, INSERM U1028, Claude Bernard Lyon 1 University, Lyon, France.; Department of Genetics, Groupement Hospitalier Est, Hospices Civils de Lyon, Claude Bernard Lyon 1 University, Lyon, France.; Lesage A; Department of Medical Imaging, CHU Sainte-Justine, Montréal, QC, Canada.; Massoud M; Department of Gynecology and Obstetrics, Multidisciplinary Center for Prenatal Diagnosis, CHLS, Hospices Civils de Lyon, Lyon, France.; Guibaud L; Pediatric and Fetal Imaging Department, Femme-Mère-Enfant Hospital, Hospices Civils de Lyon, Claude Bernard Lyon 1 University, Lyon, France.; Multidisciplinary Center for Prenatal Diagnosis, Femme-Mère-Enfant Hospital, Hospices Civils de Lyon, Claude Bernard Lyon 1 University, Lyon, France.

Publisher: John Wiley & Sons, Ltd Country of Publication: England NLM ID: 9108340 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1469-0705 (Electronic) Linking ISSN: 09607692 NLM ISO Abbreviation: Ultrasound Obstet Gynecol Subsets: MEDLINE

van der Sluijs PJ; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.; Gösgens M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.; Dingemans AJM; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.; Striano P; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy.; Riva A; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy.; IRCCS Istituto Giannina Gaslini, Genova, Italy.; Mignot C; Service de génétique médicale, APHP Pitié-Salpêtrière, Paris, France.; Faudet A; Département de Génétique, Assistance publique - Hôpitaux de Paris Sorbonne Université, Hôpital Pitié-Salpêtrière et Trousseau, Paris, France.; Vasileiou G; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.; Centre for Rare Diseases Erlangen (ZSEER), Erlangen, Germany.; Walther M; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.; Schrier Vergano SA; Children's Hospital of The King's Daughters, Norfolk, VA.; Department of Pediatrics, Eastern Virginia Medical School, Norfolk, VA.; Alders M; Section Clinical Genetics, Department of Human Genetics, Amsterdam University Medical Centers, Amsterdam, the Netherlands.; Alkuraya FS; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.; Alorainy I; Department of Radiology and Diagnostic Imaging, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia.; Alsaif HS; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Centre of Excellence for Biomedicine, Joint Centers of Excellence Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.; Anderlid B; Clinical Genetics Karolinska Universitet Hospital and Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.; Bache I; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.; van Beek I; Section Clinical Genetics, Department of Human Genetics, Amsterdam University Medical Centers, Amsterdam, the Netherlands.; Blanluet M; Service de Génétique Oncologique, Institut Curie, Paris, France.; van Bon BW; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.; Brunet T; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.; Department of Pediatric Neurology and Developmental Medicine and LMU Center for Children with Medical Complexity, Dr. von Hauner Children's Hospital, LMU Hospital, Ludwig-Maximilians-University, D-80337 Munich, Germany.; Brunner H; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.; Carriero ML; Medical Genetics, University of Siena, Siena, Italy.; Charles P; Service de génétique médicale, APHP Pitié-Salpêtrière, Paris, France.; Chatron N; Service de génétique, Hospices Civils de Lyon ERN ITHACA, INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, GENDEV Team, Université Claude Bernard Lyon 1, Bron, France.; Institut Neuromyogène, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, Equipe Métabolisme énergétique et développement neuronal, CNRS UMR 5310, INSERM U1217, Université Lyon 1, Lyon, France.; Coccia E; Department of Medical and Surgical Science, Postgraduate School of Medical Genetics, Alma Mater Studiorum University of Bologna, Bologna, Italy.; Dubourg C; Service de Génétique Moléculaire et Génomique Médicale, CHU de Rennes, Rennes, France.; Univ Rennes, CNRS, INSERM, IGDR (Institut de génétique et développement de Rennes) - UMR 6290, ERL U1305, RENNES, France.; Earl RK; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA.; Eichler EE; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA.; Howard Hughes Medical Institute, University of Washington, School of Medicine, Seattle, WA.; Faivre L; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, CHU Dijon, Dijon, France.; Genetics of Developmental Disorders, INSERM - Bourgogne Franche-Comté University, UMR 1231 GAD Team, Dijon, France.; Foulds N; Wessex Clinical Genetics Service, University Hospital Southampton, Princess Anne Hospital, Southampton, United Kingdom.; Graziano C; Medical Genetics Unit, AUSL Romagna, Cesena, Italy.; Guerrot AM; Department of Genetics and reference Center for Developmental Disorders, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, France.; Hashem MO; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Heide S; Département de Génétique, Assistance publique - Hôpitaux de Paris Sorbonne Université, Hôpital Pitié-Salpêtrière et Trousseau, Paris, France.; Heron D; Département de Génétique, Assistance publique - Hôpitaux de Paris Sorbonne Université, Hôpital Pitié-Salpêtrière et Trousseau, Paris, France.; Hickey SE; Division of Genetic & Genomic Medicine, Nationwide Children's Hospital, Columbus, OH.; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, OH.; Hopman SMJ; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; Kattentidt-Mouravieva A; Stichting Zuidwester, Middelharnis, the Netherlands.; Kerkhof J; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON, Canada.; Klein Wassink-Ruiter JS; Department of Genetics, University of Groningen, University Medical Center Groningen, the Netherlands.; Kurtz-Nelson EC; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA.; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN.; Kušíková K; Department of Pediatric Neurology, Faculty of Medicine, Comenius University and National Institute of Children's Diseases, Bratislava, Slovakia.; Kvarnung M; Clinical Genetics Karolinska Universitet Hospital and Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.; Lecoquierre F; Department of Genetics and reference Center for Developmental Disorders, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, France.; Leszinski GS; Institute of Human Genetics, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.; Loberti L; Medical Genetics, University of Siena, Siena, Italy.; Department of Medical Biotechnologies, Med Biotech Hub and Competence Centre, University of Siena, Siena, Italy.; Magoulas PL; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.; Mari F; Medical Genetics, University of Siena, Siena, Italy.; Maystadt I; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.; Merla G; Department of Molecular Medicine & Medical Biotechnology, University of Naples Federico II, Naples, Italy.; Laboratory of Regulatory & Functional Genomics, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Foggia, Italy.; Milunsky JM; Center for Human Genetics Inc, Cambridge, MA.; Moortgat S; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.; Nicolas G; Department of Genetics and reference Center for Developmental Disorders, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, France.; Leary MO'; Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard, Cambridge, MA.; Odent S; Univ Rennes, CNRS, INSERM, IGDR (Institut de génétique et développement de Rennes) - UMR 6290, ERL U1305, RENNES, France.; Centre de Référence Maladies Rares CLAD-Ouest, ERN-ITHACA, FHU GenOMedS, CHU de Rennes, RENNES, France.; Ozmore JR; Medical Genetics, Dartmouth Hitchcock Medical Center, Lebanon, NH.; Parbhoo K; Division of Genetic & Genomic Medicine, Nationwide Children's Hospital, Columbus, OH.; The Steve and Cindy Rasmussen Institute for Genomic Medicine at Nationwide Children's Hospital, Columbus, OH.; Pfundt R; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.; Piccione M; Medical Genetics Unit, AOOR Villa Sofia-Cervello Hospitals, Palermo, Italy.; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.; Pinto AM; Medical Genetics, University of Siena, Siena, Italy.; Popp B; Berlin Institute of Health at Charitè, Universitätsklinikum Berlin, Centre of Functional Genomics, Berlin, Germany.; Putoux A; Service de génétique, Hospices Civils de Lyon ERN ITHACA, INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, GENDEV Team, Université Claude Bernard Lyon 1, Bron, France.; Rehm HL; Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard, Cambridge, MA.; Reis A; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.; Centre for Rare Diseases Erlangen (ZSEER), Erlangen, Germany.; Renieri A; Medical Genetics, University of Siena, Siena, Italy.; Department of Medical Biotechnologies, Med Biotech Hub and Competence Centre, University of Siena, Siena, Italy.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.; Baylor Genetics Laboratories, Houston, TX.; Rossi M; Service de génétique, Hospices Civils de Lyon ERN ITHACA, INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, GENDEV Team, Université Claude Bernard Lyon 1, Bron, France.; Salzano E; Medical Genetics Unit, AOOR Villa Sofia-Cervello Hospitals, Palermo, Italy.; Saugier-Veber P; Department of Genetics and reference Center for Developmental Disorders, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, France.; Seri M; Department of Medical and Surgical Science, Postgraduate School of Medical Genetics, Alma Mater Studiorum University of Bologna, Bologna, Italy.; Severi G; Department of Medical and Surgical Science, Postgraduate School of Medical Genetics, Alma Mater Studiorum University of Bologna, Bologna, Italy.; Sonmez FM; Department of Child Neurology, Karadeniz Technical University Faculty of Medicine, Retired Lecturer, Trabzon, Turkey.; Strobl-Wildemann G; MVZ Humangenetik Ulm, Ulm, Germany.; Stuurman KE; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.; Uctepe E; Acıbadem Labmed Ankara Tissue Typing Laboratory, Ankara, Turkey.; Van Esch H; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.; Vitetta G; Department of Medical and Surgical Science, Postgraduate School of Medical Genetics, Alma Mater Studiorum University of Bologna, Bologna, Italy.; de Vries BBA; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.; Wahl D; Department of Clinical Genetics, MVZ Martinsried, Munich, Germany.; Wang T; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA.; Department of Medical Genetics, Center for Medical Genetics, School of Basic Medical Sciences, Peking University, Beijing, China.; Neuroscience Research Institute, Peking University Key Laboratory for Neuroscience, Ministry of Education of China & National Health Commission of China, Beijing, China.; Autism Research Center, Peking University Health Science Center, Beijing, China.; Zacher P; Epilepsy Center Kleinwachau, Radeberg, Germany.; Heitink KR; Department of Rehabilitation Medicine, Leiden University Medical Center, Leiden, the Netherlands.; Ropers FG; Willem-Alexander Children's Hospital, department of Pediatrics, Leiden University Medical Center, the Netherlands.; Steenbeek D; Department of Rehabilitation Medicine, Maastricht University Medical Center / Adelante Rehabilitation, Maastricht, The Netherlands.; Rybak T; 's Heeren Loo Noordwijk, Noordwijk, the Netherlands.; Santen GWE; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.

Publisher: Elsevier Inc Country of Publication: United States NLM ID: 9918734281906676 Publication Model: eCollection Cited Medium: Internet ISSN: 2949-7744 (Electronic) Linking ISSN: 29497744 NLM ISO Abbreviation: Genet Med Open Subsets: PubMed not MEDLINE

Nguyen, K; Putoux, A; Busa, Tiffany; Cordier, M P; Sigaudy, Sabine; Till, M; Chabrol, B; Michel-Calemard, L; Bernard, R; Julia, S; Malzac, P; Labalme, A; Missirian, C; Edery, P; Popovici, C; Philip, N; Sanlaville, D

Clinical Genetics. 87:488-491

Attié-Bitach, T; Beales, PL; Vekemans, M; Gonzales, M; Katsanis, N; Winey, M; Siffroi, JP; Encha-Razavi, F; Lyonnet, S; Goudin, N; Schmitt, A; Cagnard, N; Bole-Feysot, C; Akarsu, NA; Colin, E; Hennekam, R; Cormier-Daire, V; Munnich, A; Thauvin-Robinet, C; Fertitta, L; Nitschke, P; Boduroglu, K; Utine, GE; Pruvost, S; Joyé, N; Rigonnot, L; Frison, MH; Elkhartoufi, N; Bennett, CL; Patrier, S; Gomes, C; Buzas, D; Uz, ELİF; Ogur, G; Alanay, Y; Davis, EE; Coene, KL; Thomas, S; Putoux, A

Nature Genetics. 43:601-606

Gokce-Samar Z; Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, Member of ERN-EpiCARE; HFME, University Hospitals of Lyon (HCL), Lyon, France. Electronic address: zeynep.gokce-samar@chu-lyon.fr.; de Bellescize J; Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, Member of ERN-EpiCARE; HFME, University Hospitals of Lyon (HCL), Lyon, France.; Arzimanoglou A; Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, Member of ERN-EpiCARE; HFME, University Hospitals of Lyon (HCL), Lyon, France.; Putoux A; Department of Genetics; HFME, Member of ERN-EpiCARE; University Hospitals of Lyon (HCL), Lyon, France.; Chatron N; Department of Genetics; HFME, Member of ERN-EpiCARE; University Hospitals of Lyon (HCL), Lyon, France.; Lesca G; Department of Genetics; HFME, Member of ERN-EpiCARE; University Hospitals of Lyon (HCL), Lyon, France.; Portes VD; Department of Pediatric Neurology; Member of ERN-EpiCARE; Rare Disease Reference Centre for Intellectual Disability, University Hospitals of Lyon (HCL), And University Lyon1, Lyon, France.

Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE

Putoux A; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Centre de Recherche en Neurosciences de Lyon, INSERM U1028, UMR CNRS 5292, Université Claude Bernard Lyon 1, Lyon, France.; Alqahtani A; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Pinson L; Département de Génétique Médicale, Centre Hospitalier Universitaire, Montpellier, France.; Paulussen AD; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, the Netherlands.; School for Oncology & Developmental Biology (GROW), Maastricht University Medical Centre, Maastricht, the Netherlands.; Michel J; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Besson A; Centre de Recherche en Neurosciences de Lyon, INSERM U1028, UMR CNRS 5292, Université Claude Bernard Lyon 1, Lyon, France.; Mazoyer S; Centre de Recherche en Neurosciences de Lyon, INSERM U1028, UMR CNRS 5292, Université Claude Bernard Lyon 1, Lyon, France.; Borg I; Department of Pathology, University of Malta, Medical Genetics Unit, Mater Dei Hospital, Malta.; Nampoothiri S; Department of Paediatric Genetics, Amrita Institute of Medical Sciences and Research Centre, Cochin, India.; Vasiljevic A; Centre de Pathologie et Neuropathologie Est, Hospices Civils de Lyon, Lyon, France.; Uwineza A; Centre for Medical Genetics, College of Medicine and Health Sciences, University of Rwanda, Huye, Rwanda.; Boggio D; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Champion F; Service de Gynécologie-Obstétrique, Hospices Civils de Lyon, Lyon, France.; de Die-Smulders CE; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, the Netherlands.; School for Oncology & Developmental Biology (GROW), Maastricht University Medical Centre, Maastricht, the Netherlands.; Gardeitchik T; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, the Netherlands.; van Putten WK; Paediatric Intensive Care Unit, Radboud University Medical Centre, Nijmegen, the Netherlands.; Perez MJ; Département de Génétique Médicale, Unité de fœtopathologie, Centre Hospitalier Universitaire, Montpellier, France.; Musizzano Y; Département de Pathologie Tissulaire et Cellulaire des tumeurs, Pôle Biologie Pathologie, Centre Hospitalier Universitaire, Montpellier, France.; Razavi F; Département de Génétique Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfant Malade, Paris, France.; Drunat S; Department of Genetics, APHP-Robert DEBRE University Hospital, and Paris-Diderot University, Paris, France.; Verloes A; Department of Genetics, APHP-Robert DEBRE University Hospital, and Paris-Diderot University, Paris, France.; Hennekam R; Department of Paediatrics, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.; Guibaud L; Département d'Imagerie Pédiatrique et Fœtale, Centre Pluridisciplinaire de Diagnostic Prénatal, Hôpital Femme Mère Enfant, Lyon-Bron, France.; Alix E; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Sanlaville D; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Centre de Recherche en Neurosciences de Lyon, INSERM U1028, UMR CNRS 5292, Université Claude Bernard Lyon 1, Lyon, France.; Lesca G; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Centre de Recherche en Neurosciences de Lyon, INSERM U1028, UMR CNRS 5292, Université Claude Bernard Lyon 1, Lyon, France.; Edery P; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Centre de Recherche en Neurosciences de Lyon, INSERM U1028, UMR CNRS 5292, Université Claude Bernard Lyon 1, Lyon, France.

Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

Nizon M; Département de Génétique, Université Paris Descartes-Sorbonne Paris Cité, INSERM UMR1163, Institut IMAGINE, Hôpital Necker-Enfants Malades, Paris, France.; Henry M; Département de Génétique, Université Paris Descartes-Sorbonne Paris Cité, INSERM UMR1163, Institut IMAGINE, Hôpital Necker-Enfants Malades, Paris, France.; Michot C; Département de Génétique, Université Paris Descartes-Sorbonne Paris Cité, INSERM UMR1163, Institut IMAGINE, Hôpital Necker-Enfants Malades, Paris, France.; Baumann C; Département de Génétique, CHU Robert Debré, Paris, France.; Bazin A; Département de Génétique, CH René Dubos, Pontoise, France.; Bessières B; Département de Génétique, Université Paris Descartes-Sorbonne Paris Cité, INSERM UMR1163, Institut IMAGINE, Hôpital Necker-Enfants Malades, Paris, France.; Blesson S; Service de Génétique, CHRU Tours, Hôpital Bretonneau, Tours, France.; Cordier-Alex MP; Service de Génétique Clinique, Hospices Civils de Lyon, Bron, France.; David A; Service de Génétique Médicale, CHU, Nantes, France.; Delahaye-Duriez A; Service de Génétique, CHU Paris Seine-Saint-Denis, Hôpital Jean Verdier, Bondy, France.; Delezoïde AL; Département de Génétique, CHU Robert Debré, Paris, France.; Dieux-Coeslier A; Service de Génétique Clinique, CHRU de Lille, Hôpital Jeanne de Flandre, Lille, France.; Doco-Fenzy M; Service de Génétique, CHU de Reims, Hôpital Maison Blanche, Reims, France.; Faivre L; Centre de Génétique, CHU de Dijon, Dijon, France.; Goldenberg A; Département de Génétique, CHU, Rouen, France.; Layet V; Service de Génétique Médicale, GH du Havre, Hôpital Jacques Monod, Le Havre, France.; Loget P; Service d'anatomie et cytologie pathologiques, Hôpital Pontchaillou, Université de Rennes 1, CHU, Rennes, France.; Marlin S; Département de Génétique, Université Paris Descartes-Sorbonne Paris Cité, INSERM UMR1163, Institut IMAGINE, Hôpital Necker-Enfants Malades, Paris, France.; Martinovic J; Département de Génétique, Université Paris Descartes-Sorbonne Paris Cité, INSERM UMR1163, Institut IMAGINE, Hôpital Necker-Enfants Malades, Paris, France.; Odent S; Service de Génétique Clinique, CHU Rennes, Hôpital Sud, Rennes, France.; Pasquier L; Service de Génétique Clinique, CHU Rennes, Hôpital Sud, Rennes, France.; Plessis G; Service de Génétique Médicale, CHU Clémenceau, Caen, France.; Prieur F; Service de Génétique Clinique, CHU de Saint-Etienne, Hôpital Nord, Saint-Priest-en-Jarez, France.; Putoux A; Service de Génétique Clinique, Hospices Civils de Lyon, Bron, France.; Rio M; Département de Génétique, Université Paris Descartes-Sorbonne Paris Cité, INSERM UMR1163, Institut IMAGINE, Hôpital Necker-Enfants Malades, Paris, France.; Testard H; Département de Pédiatrie, CHU Grenoble, Grenoble, France.; Bonnefont JP; Département de Génétique, Université Paris Descartes-Sorbonne Paris Cité, INSERM UMR1163, Institut IMAGINE, Hôpital Necker-Enfants Malades, Paris, France.; Cormier-Daire V; Département de Génétique, Université Paris Descartes-Sorbonne Paris Cité, INSERM UMR1163, Institut IMAGINE, Hôpital Necker-Enfants Malades, Paris, France.

Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

Lacalm A; Département d'Imagerie Pédiatrique et Fœtale, Hôpital Femme Mère Enfant, Lyon-Bron, France.; Nadaud B; Laboratoire de Pathologie, Hôpital Femme Mère Enfant, Lyon-Bron, France.; Massoud M; Centre Pluridisciplinaire de Diagnostic Prénatal, Hôpital Femme Mère Enfant, Lyon-Bron, France.; Putoux A; Département de Génétique, Hôpital Femme Mère Enfant, Lyon-Bron, France.; Gaucherand P; Centre Pluridisciplinaire de Diagnostic Prénatal, Hôpital Femme Mère Enfant, Lyon-Bron, France.; Guibaud L; Département d'Imagerie Pédiatrique et Fœtale, Hôpital Femme Mère Enfant, Lyon-Bron, France.; Centre Pluridisciplinaire de Diagnostic Prénatal, Hôpital Femme Mère Enfant, Lyon-Bron, France.

Publisher: John Wiley & Sons, Ltd Country of Publication: England NLM ID: 9108340 Publication Model: Print Cited Medium: Internet ISSN: 1469-0705 (Electronic) Linking ISSN: 09607692 NLM ISO Abbreviation: Ultrasound Obstet Gynecol Subsets: MEDLINE