부산대학교 도서관

Morris, Joan K.; Bergman, Jorieke E. H.; Barisic, Ingeborg; Wellesley, Diana; Tucker, David; Limb, Elizabeth; Addor, Marie-Claude; Cavero-Carbonell, Clara; Matias Dias, Carlos; Draper, Elisabeth S.; Echevarría-González-de-Garibay, Luis Javier; Gatt, Miriam; Klungsøyr, Kari; Lelong, Nathalie; Luyt, Karen; Materna-Kiryluk, Anna; Nelen, Vera; Neville, Amanda; Perthus, Isabelle; Pierini, Anna; Randrianaivo-Ranjatoelina, Hanitra; Rankin, Judith; Rissmann, Anke; Rouget, Florence; Sayers, Geraldine; Wertelecki, Wladimir; Kinsner-Ovaskainen, Agnieszka; Garne, Ester

European Journal of Human Genetics. 32(4):407-412

Arnaud C; CERPOP, UMR 1295 Toulouse University, Inserm, Paul Sabatier University, Toulouse, France.; Childhood Disability Registry in Haute-Garonne, University Hospital of Toulouse, Toulouse, France.; Clinical Epidemiology Unit, University Hospital of Toulouse, Toulouse, France.; Ehlinger V; CERPOP, UMR 1295 Toulouse University, Inserm, Paul Sabatier University, Toulouse, France.; Childhood Disability Registry in Haute-Garonne, University Hospital of Toulouse, Toulouse, France.; Perraud A; European Commission, Joint Research Centre, Ispra, Italy.; Kinsner-Ovaskainen A; European Commission, Joint Research Centre, Ispra, Italy.; Klapouszczak D; CERPOP, UMR 1295 Toulouse University, Inserm, Paul Sabatier University, Toulouse, France.; Childhood Disability Registry in Haute-Garonne, University Hospital of Toulouse, Toulouse, France.; Himmelmann K; Department of Pediatrics, Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Petra M; Department of Orthopaedics, General Hospital of Syros, Syros, Greece.; Rackauskaite G; Child and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.; Lanzoni M; European Commission, Joint Research Centre, Ispra, Italy.; Platt MJ; Norwich Medical School, University of East Anglia, Norwich, UK.; Delobel-Ayoub M; CERPOP, UMR 1295 Toulouse University, Inserm, Paul Sabatier University, Toulouse, France.; Childhood Disability Registry in Haute-Garonne, University Hospital of Toulouse, Toulouse, France.

Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 8709766 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-3016 (Electronic) Linking ISSN: 02695022 NLM ISO Abbreviation: Paediatr Perinat Epidemiol Subsets: MEDLINE

Coi A; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.; Barisic I; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.; Garne E; Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.; Pierini A; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.; Fondazione Toscana Gabriele Monasterio, Pisa, Italy.; Addor MC; Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.; Aizpurua Atxega A; Public Health Division of Gipuzkoa, Biodonostia Research Institute, Donostia-San Sebastian, Spain.; Ballardini E; Neonatal Intensive Care Unit, Paediatric Section, IMER Registry (Emilia Romagna Registry of Birth Defects), Department of Medical Sciences, University of Ferrara, Ferrara, Italy.; Braz P; Epidemiology Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.; Broughan JM; National Congenital Anomaly and Rare Disease Registration Service, National Disease Registration Service, NHS Digital, Leeds, UK.; Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.; de Walle HEK; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.; Draper ES; Department Health Sciences, College of Life Sciences, University of Leicester, Leicester, UK.; Gatt M; Malta Congenital Anomalies Registry, Directorate for Health Information and Research, G'Mangia, Malta.; Häusler M; Medical University of Graz, Graz, Austria.; Kinsner-Ovaskainen A; European Commission, Joint Research Centre (JRC), Ispra, Italy.; Kurinczuk JJ; National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.; Lelong N; Université Paris Cité, Inserm, INRAE, Centre for Research in Epidemiology and StatisticS (CRESS), Obstetrical Perinatal and Pediatric Epidemiology Research Team, EPOPé, Paris, France.; Luyt K; South West Congenital Anomaly Register, Bristol Medical School, University of Bristol, Bristol, UK.; Mezzasalma L; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.; Mullaney C; Department of Public Health, HSE South East, Lacken, Kilkenny, Ireland.; Nelen V; Provincial Institute of Hygiene, Antwerp, Belgium.; Odak L; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.; O'Mahony MT; Department of Public Health, HSE South (Cork & Kerry), Cork, Ireland.; Perthus I; Auvergne Registry of Congenital Anomalies (CEMC-Auvergne), Department of Clinical Genetics, Centre de Référence des Maladies Rares, University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.; Randrianaivo H; Register of Congenital Malformations Isle of Reunion Island, CHU St Pierre, la Reunion, Reunion, France.; Rankin J; National Congenital Anomaly and Rare Disease Registration Service, National Disease Registration Service, NHS Digital, Leeds, UK.; Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.; Rissmann A; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke University, Magdeburg, Germany.; Rouget F; Brittany Registry of Congenital Anomalies, CHU Rennes, Univ Rennes, Inserm, EHESP, IRSET (Institut de Recherche en Santé, Environnement et Travail) - UMR_S 1085, Rennes, France.; Schaub B; French West Indies Registry, Registre des Malformations des Antilles (REMALAN), Maison de la Femme de la Mère et de l'Enfant, University Hospital of Martinique, Fort-de-France, France.; Tucker D; Congenital Anomaly Register & Information Service for Wales (CARIS), Public Health Wales, Swansea, UK.; Wellesley D; University Hospital Southampton, Faculty of Medicine and Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.; Wiśniewska K; Epidemiology Unit, Department of Preventive Medicine, Poznan University of Medical Sciences, Poznan, Poland.; Yevtushok L; OMNI-Net Ukraine Birth Defects Program and Rivne Regional Medical Diagnostic Center, Rivne, Ukraine.; Santoro M; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.

Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 9216037 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-3083 (Electronic) Linking ISSN: 09269959 NLM ISO Abbreviation: J Eur Acad Dermatol Venereol Subsets: MEDLINE

Morris JK; St George's, University of London, London, United Kingdom.; Wellesley D; Clinical Genetics, University of Southampton and Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom.; Limb E; St George's, University of London, London, United Kingdom.; Bergman JEH; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.; Kinsner-Ovaskainen A; European Commission, Joint Research Centre (JRC), Ispra, Italy.; Addor MC; Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.; Broughan JM; National Disease Registration Service, NHS Digital, Leeds, United Kingdom.; Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.; Dias CM; Department of Epidemiology, Instituto Nacional de Saúde Doutor Ricardo Jorge; Av padre Cruz, Lisbon, Portugal.; Echevarría-González-de-Garibay LJ; Ministry of Health of the Basque Government, Directorate for Healthcare Planning, Organisation and Evaluation, Vitoria-Gasteiz, Spain.; Gatt M; Directorate for Health Information and Research, Malta Congenital Anomalies Registry, G'Mangia, Malta.; Haeusler M; Medical University of Graz, Austria.; Barisic I; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.; Klungsoyr K; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.; Division of Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway.; Lelong N; Université de Paris, INSERM U1153, CRESS, Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOPé), Paris, France.; Materna-Kiryluk A; Polish Registry of Congenital Malformations, Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.; Neville A; Center for Clinical and Epidemiological Research, University of Ferrara, Ferrara, Italy.; Nelen V; Provincial Institute for Hygiene, Antwerp, Belgium.; O'Mahony MT; Department of Public Health, Health Service Executive-South, Cork, Ireland.; Perthus I; Auvergne Registry of Congenital Anomalies (CEMC-Auvergne), Department of Clinical Genetics, Centre de Référence des Maladies Rares, University Hospital of Clermont-Ferrand, CNRS-UMR 6602, Institut Pascal, Axe TGI, équipe PEPRADE, Clermont-Ferrand, France.; Pierini A; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.; Fondazione Toscana Gabriele Monasterio, Pisa, Italy.; Rankin J; Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.; Rissmann A; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.; Rouget F; Brittany Registry of Congenital Anomalies, CHU Rennes, Univ Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, Rennes, France.; Sayers G; Health Intelligence, Research and Development Health Service Executive, Dublin, Ireland.; Stevens S; National Disease Registration Service, NHS Digital, Leeds, United Kingdom.; Tucker D; Public Health Knowledge and Research, Public Health Wales, Singleton Hospital, Swansea, United Kingdom.; Garne E; Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.

Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101701004 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2472-1727 (Electronic) NLM ISO Abbreviation: Birth Defects Res Subsets: MEDLINE

Bergman, Jorieke E. H.; Perraud, Annie; Barisic, Ingeborg; Kinsner-Ovaskainen, Agnieszka; Morris, Joan K.; Tucker, David; Wellesley, Diana; Garne, Ester

BIRTH DEFECTS RESEARCH; FEB 2024, 116 2, pe2314 20p.

Morris JK; Population Health Research Institute, St. George's, University of London, London, United Kingdom.; Addor MC; Department of Woman-Mother-Child, University Hospital Center, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.; Ballardini E; Indagine Sulle Malformazioni Congenite in Emilia-Romagna (IMER) Registry (Emilia Romagna Registry of Birth Defects) Neonatal Intensive Care Unit, Pediatric Section Department of Medical Sciences, University of Ferrara, Ferrara, Italy.; Barisic I; Centre of Excellence for Reproductive and Regenerative Medicine, Children's Hospital Zagreb, Medical School University of Zagreb, Zagreb, Croatia.; Barrachina-Bonet L; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.; Braz P; Epidemiology Department, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal.; Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.; Den Hond E; Health Department, Provincial Institute of Hygiene, Antwerp, Belgium.; Garne E; Paediatric Department, Hospital Lillebaelt Kolding, Kolding, Denmark.; Gatt M; Directorate for Health Information and Research, Pietà, Malta.; Haeusler M; Department of Obstetrics and Gynaecology, Medical University of Graz, Graz, Austria.; Khoshnood B; Université de Paris, Center of Research in Epidemiology and StatisticS/CRESS/Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOPé), INSERM, INRA, Paris, France.; Lelong N; Université de Paris, Center of Research in Epidemiology and StatisticS/CRESS/Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOPé), INSERM, INRA, Paris, France.; Kinsner-Ovaskainen A; European Commission, Joint Research Centre, Ispra, Italy.; Kiuru-Kuhlefelt S; Finnish Institute for Health and Welfare Terveyden Ja Hyvinvoinnin Laitos (THL), Register of Congenital Malformations, Helsinki, Finland.; Klungsoyr K; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.; Division of Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway.; Latos-Bielenska A; Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.; Limb E; Population Health Research Institute, St. George's, University of London, London, United Kingdom.; O'Mahony MT; Health Service Executive-South, Department of Public Health, St. Finbarr's Hospital, Cork, Ireland.; Perthus I; Auvergne Registry of Congenital Anomalies (CEMC-Auvergne), Department of Clinical Genetics, Centre de Référence des Maladies Rares, CHU Estaing, Clermont-Ferrand, France.; Pierini A; Institute of Clinical Physiology, National Research Council, Pisa, Italy.; Rankin J; Population Health Sciences Institute, Newcastle University, Newcastle, United Kingdom.; Rissmann A; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke-University, Magdeburg, Germany.; Rouget F; Brittany Registry of Congenital Anomalies, CHU Rennes, Univ Rennes, INSERM, EHESP, Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, Rennes, France.; Sayers G; Health Intelligence R&D Health Service Executive, Dublin, Ireland.; Sipek A Jr; Department of Medical Biology and Genetics, 1st Faculty of Medicine, General University Hospital, Charles University, Prague, Czechia.; Stevens S; Public Health England, London, United Kingdom.; Tucker D; Congenital Anomaly Register and Information Service for Wales, Public Health Wales Knowledge Directorate, Singleton Hospital, Swansea, United Kingdom.; Verellen-Dumoulin C; Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Charleroi, Belgium.; de Walle HEK; Department of Genetics, Eurocat Northern Netherlands, University of Groningen, University Medical Center Groningen, Groningen, Netherlands.; Wellesley D; Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom.; Wertelecki W; OMNI-Net Ukraine Programs, Rivne, Ukraine.; Bermejo-Sanchez E; Spanish Collaborative Study of Congenital Malformations (ECEMC), Unidad de Investigación sobre Anomalías Congénitas, Institute of Rare Diseases Research (IIER), Instituto de Salud Carlos III, Madrid, Spain.

Publisher: Frontiers Media SA Country of Publication: Switzerland NLM ID: 101615492 Publication Model: eCollection Cited Medium: Print ISSN: 2296-2360 (Print) Linking ISSN: 22962360 NLM ISO Abbreviation: Front Pediatr Subsets: PubMed not MEDLINE

Morris, Joan K.; Bergman, Jorieke E. H.; Barisic, Ingeborg; Wellesley, Diana; Tucker, David; Limb, Elizabeth; Addor, Marie-Claude; Cavero-Carbonell, Clara; Dias, Carlos Matias; Draper, Elisabeth S.; Echevarria-Gonzalez-de-Garibay, Luis Javier; Gatt, Miriam; Klungsoyr, Kari; Lelong, Nathalie; Luyt, Karen; Materna-Kiryluk, Anna; Nelen, Vera; Neville, Amanda; Perthus, Isabelle; Pierini, Anna; Randrianaivo-Ranjatoelina, Hanitra; Rankin, Judith; Rissmann, Anke; Rouget, Florence; Sayers, Geraldine; Wertelecki, Wladimir; Kinsner-Ovaskainen, Agnieszka; Garne, Ester

EUROPEAN JOURNAL OF HUMAN GENETICS; DEC 5 2023, 6p.

Santoro, Michele; Coi, Alessio; Barisic, Ingeborg; Garne, Ester; Addor, Marie-Claude; Bergman, Jorieke E.H.; Bianchi, Fabrizio; Boban, Ljubica; Braz, Paula; Cavero-Carbonell, Clara; Gatt, Miriam; Haeusler, Martin; Kinsner-Ovaskainen, Agnieszka; Klungsoyr, Kari; Kurinczuk, Jennifer J.; Lelong, Nathalie; Luyt, Karen; Materna-Kiryluk, Anna

Neuroepidemiology. November 1, 2019, Vol. 53 Issue 3-4, p169, 11 p.

Petersen EJ; Biosystems and Biomaterials Division, Material Measurement Laboratory, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland 20899, United States.; Hirsch C; Particles-Biology Interactions Laboratory, Empa, Swiss Federal Laboratories for Material Science and Technology, CH-9014 St. Gallen, Switzerland.; Elliott JT; Biosystems and Biomaterials Division, Material Measurement Laboratory, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland 20899, United States.; Krug HF; NanoCASE GmbH, St. Gallerstr. 58, 9032 Engelburg, Switzerland.; Aengenheister L; Particles-Biology Interactions Laboratory, Empa, Swiss Federal Laboratories for Material Science and Technology, CH-9014 St. Gallen, Switzerland.; Arif AT; Institute for Infection Prevention and Hospital Epidemiology, University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, D-79106 Freiburg, Germany.; Kurdistan Institution for Strategic Studies and Scientific Research (KISSR), Qirga, Sulaimani, Iraq.; Bogni A; European Commission, Joint Research Centre (JRC), 21027 Ispra, Italy.; Kinsner-Ovaskainen A; European Commission, Joint Research Centre (JRC), 21027 Ispra, Italy.; May S; Particles-Biology Interactions Laboratory, Empa, Swiss Federal Laboratories for Material Science and Technology, CH-9014 St. Gallen, Switzerland.; Walser T; Vereala GmbH, Eyhof 34, 8047 Zürich, Switzerland.; Wick P; Particles-Biology Interactions Laboratory, Empa, Swiss Federal Laboratories for Material Science and Technology, CH-9014 St. Gallen, Switzerland.; Roesslein M; Particles-Biology Interactions Laboratory, Empa, Swiss Federal Laboratories for Material Science and Technology, CH-9014 St. Gallen, Switzerland.

Publisher: American Chemical Society Country of Publication: United States NLM ID: 8807448 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1520-5010 (Electronic) Linking ISSN: 0893228X NLM ISO Abbreviation: Chem Res Toxicol Subsets: MEDLINE

van de Putte R; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud university medical center (Radboudumc), Nijmegen, The Netherlands.; van Rooij IALM; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud university medical center (Radboudumc), Nijmegen, The Netherlands.; Paediatric Surgery, Radboudumc Amalia Children's Hospital, Nijmegen, The Netherlands.; Haanappel CP; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud university medical center (Radboudumc), Nijmegen, The Netherlands.; Marcelis CLM; Department of Human Genetics, Nijmegen, The Netherlands.; Brunner HG; Department of Human Genetics, Nijmegen, The Netherlands.; Department of Clinical Genetics and School for Oncology & Developmental Biology (GROW), Maastricht University Medical Center, Maastricht, The Netherlands.; Addor MC; Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.; Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.; Dias CM; Epidemiology Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.; Draper ES; Department of Health Sciences, University of Leicester, Leicester, UK.; Etxebarriarteun L; Department of Health, Public Health Service, Basque Government Basque Country, Vitoria-Gasteiz, Spain.; Gatt M; Malta Congenital Anomalies Register, Directorate for Health Information and Research, Pietà, Malta.; Khoshnood B; INSERM UMR 1153, Obstetrical, Perinatal and Pediatric Epidemiology Research Team (EPOPé), Center of Research in Epidemiology and Statistics Sorbonne Paris Cité (CRESS), DHU Risks in Pregnancy, Paris Descartes University, Paris, France.; Kinsner-Ovaskainen A; European Commission, Joint Research Centre (JRC), Ispra, Italy.; Klungsoyr K; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.; Division for Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway.; Kurinczuk JJ; National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.; Latos-Bielenska A; Department of Medical Genetics, University of Medical Sciences, Poznań, Poland.; Luyt K; South West Congenital Anomaly Register (SWCAR), Bristol Medical School, University of Bristol, Bristol, UK.; O'Mahony MT; Department of Public Health, Health Service Executive - South, Cork, Ireland.; Miller N; National Congenital Anomaly and Rare Disease Registration Service, Public Health England, Newcastle upon Tyne, UK.; Mullaney C; Department of Public Health, Health Service Executive - South East, Kilkenny, Ireland.; Nelen V; Provinciaal Instituut voor Hygiene (PIH), Antwerp, Belgium.; Neville AJ; Registro IMER - IMER Registry (Emilia Romagna Registry of Birth Defects), Center for Clinical and Epidemiological Research, University of Ferrara, Azienda Ospedaliero-Universitaria di Ferrara, Ferrara, Italy.; Perthus I; Auvergne registry of congenital anomalies (CEMC-Auvergne), Department of clinical genetics, Centre de Référence des Maladies Rares, University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.; Pierini A; Tuscany Registry of Congenital Defects (RTDC), Institute of Clinical Physiology - National Research Council / Fondazione Toscana Gabriele Monasterio, Pisa, Italy.; Randrianaivo H; Register of congenital malformations of Reunion Island, CHU Réunion, St Pierre, France.; Rankin J; Institute of Health & Society, Newcastle University, Newcastle, UK.; Rissmann A; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke University, Magdeburg, Germany.; Rouget F; Brittany Registry of congenital anomalies, CHU Rennes, University Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail), Rennes, France.; Schaub B; French West Indies Registry, Registre des Malformations des Antilles (REMALAN), Maison de la Femme de la Mère et de l'Enfant, University Hospital of Martinique, Fort-de-France, France.; Tucker D; CARIS, Public Health Wales, Singleton Hospital, Swansea, UK.; Wellesley D; Wessex Clinical Genetics Department, Princess Anne Hospital, Southampton, UK.; Wiesel A; Department of Pediatrics, Birth Registry Mainz Model, University Medical Center of Mainz, Mainz, Germany.; Zymak-Zakutnia N; OMNI-Net Ukraine Birth Defects Program and Khmelnytsky City Children's Hospital, Khmelnytsky, Ukraine.; Loane M; Centre for Maternal, Fetal and lnfant Research, lnstitute of Nursing and Health Research, Ulster University, Belfast, UK.; Barisic I; Centre of Excellence for Reproductive and Regenerative Medicine, Children's Hospital Zagreb, Medical School University of Zagreb, Zagreb, Croatia.; de Walle HEK; Department of Genetics, EUROCAT Northern Netherlands, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.; Bergman JEH; Department of Genetics, EUROCAT Northern Netherlands, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.; Roeleveld N; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud university medical center (Radboudumc), Nijmegen, The Netherlands.

Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101701004 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2472-1727 (Electronic) NLM ISO Abbreviation: Birth Defects Res Subsets: MEDLINE