부산대학교 도서관

Suh Y; Department of Chemistry, Research Institute for Natural Sciences, Hanyang University, Seoul, Korea.; Yoon CH; Department of Chemistry, Research Institute for Natural Sciences, Hanyang University, Seoul, Korea.; Kim RK; Department of Chemistry, Research Institute for Natural Sciences, Hanyang University, Seoul, Korea.; Lim EJ; Department of Chemistry, Research Institute for Natural Sciences, Hanyang University, Seoul, Korea.; Oh YS; Department of Life Science, College of Natural Sciences, Hanyang University, Seoul, Korea.; Hwang SG; Division of Radiation Cancer Biology, Korea Institute of Radiological and Medical Sciences, Seoul, Korea.; An S; Functional Genoproteome Research Centre, Konkuk University, Seoul, Korea.; Yoon G; Department of Biochemistry and Molecular Biology, Ajou University School of Medicine, Suwon, Korea.; Gye MC; Department of Life Science, College of Natural Sciences, Hanyang University, Seoul, Korea.; Yi JM; Research Center, Dongnam Institute of Radiological and Medical Sciences, Busan, Korea.; Kim MJ; Division of Radiation Cancer Biology, Korea Institute of Radiological and Medical Sciences, Seoul, Korea.; Lee SJ; Department of Chemistry, Research Institute for Natural Sciences, Hanyang University, Seoul, Korea. sj0420@hanyang.ac.kr.

Publisher: Nature Publishing Group Country of Publication: England NLM ID: 8711562 Publication Model: Print Cited Medium: Internet ISSN: 1476-5594 (Electronic) Linking ISSN: 09509232 NLM ISO Abbreviation: Oncogene Subsets: In Process; MEDLINE

Suh, Y; Yoon, C-H; Kim, R-K; Lim, E-J; Oh, Y S; Hwang, S-G; An, S; Yoon, G; Gye, M C; Yi, J-M; Kim, M-J; Lee, S-J

Oncogene. 10/10/2013, Vol. 32 Issue 41, p4873-4882. 10p.

Yang, J; Kim, HG; Song, YJ; Yoon, G; Na, YJ

In The Journal of Minimally Invasive Gynecology November-December 2015 22(6) Supplement:S194-S194

Maruyama, K; Yoon, G; Watanabe, T

IOP Conference Series: Earth & Environmental Science; Mar2019, Vol. 238, p1-7, 7p

Gonorazky, HD; Marshall, CR; Al-Murshed, M; Hazrati, L-N; Thor, MG; Hanna, MG; Mannikko, R; Ray, PN; Yoon, G

Neuromuscular Disorders. 27:574-580

Mestre, TA; Manole, A; MacDonald, H; Riazi, S; Kraeva, N; Hanna, MG; Lang, AE; Männikkö, R; Yoon, G

neurogenetics. 17:245-249

Yoon, G; Westmacott, R; MacMillan, L; Quercia, N; Koutsou, P; Georghiou, A; Christodoulou, K; Banwell, B

Journal of Neurology, Neurosurgery, & Psychiatry. Feb 01, 2008 79(2):234-236

Mezzich, J E; Ruipérez, M A; Pérez, C; Yoon, G; Liu, J; Mahmud, S

Journal of Nervous & Mental Disease; May2000, Vol. 188 Issue 5, p301-305, 5p

Kim, H; Lim, E; Jo, C; Yoon, G; Hwang, J; Jeong, S; Lee, J; Kang, K

Nano Energy. 16:62-70

Suh, Y; Yoon, C-H; Kim, R-K; Lim, E-J; Oh, Y S; Hwang, S-G; An, S; Yoon, G; Gye, M C; Yi, J-M; Kim, M-J; Lee, S-J

Oncogene. February 23, 2017, Vol. 36 Issue 8, p1167.

Rummey, C; Corben, LA; Delatycki, MB; Subramony, SH; Bushara, K; Gomez, CM; Hoyle, JC; Yoon, G; Ravina, B; Mathews, KD; Wilmot, G; Zesiewicz, T; Perlman, S; Farmer, JM; Lynch, DR

Neurol Genet

Donkervoort S; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Sabouny R; Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Canada.; Yun P; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Gauquelin L; Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Chao KR; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Boston, MA, USA.; Hu Y; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Al Khatib I; Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Canada.; Töpf A; John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.; Mohassel P; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Cummings BB; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Boston, MA, USA.; Kaur R; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Saade D; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Moore SA; Department of Pathology Carver College of Medicine, The University of Iowa, Iowa City, IA, USA.; Waddell LB; Kids Neuroscience Centre, Kids Research, The Children's Hospital at Westmead, Sydney, NSW 2145, Australia.; Discipline of Child and Adolescent Health, Faculty of Medicine and Health, The University of Sydney, Westmead, NSW 2145, Australia.; Farrar MA; Department of Neurology, Sydney Children's Hospital, Sydney, NSW, Australia.; UNSW Sydney, School of Women's and Children's Health, Sydney, NSW, Australia.; Goodrich JK; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Boston, MA, USA.; Uapinyoying P; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Research for Genetic Medicine, Children's National Medical Center, Washington, DC, USA.; Chan SHS; Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China.; Javed A; School of Biomedical Science, The University of Hong Kong, Hong Kong SAR, China.; Leach ME; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Oregon Health and Science University, Neuromuscular Program, Doernbecher Children's Hospital, Portland, OR, USA.; Karachunski P; Department of Neurology, University of Minnesota, Minneapolis, MN, USA.; Dalton J; Department of Neurology, University of Minnesota, Minneapolis, MN, USA.; Medne L; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, USA.; Harper A; Department of Neurology, Virginia Commonwealth University, Children's Hospital of Richmond at VCU, Richmond, VA, USA.; Thompson C; Department of Pediatrics, University of California San Diego, San Diego, CA, USA.; Thiffault I; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, USA.; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, USA.; Specht S; John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.; Lamont RE; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.; Saunders C; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, USA.; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, USA.; University of Missouri-Kansas City School of Medicine, Kansas City, USA.; Racher H; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.; Bernier FP; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.; Mowat D; UNSW Sydney, School of Women's and Children's Health, Sydney, NSW, Australia.; Department of Medical Genetics, Sydney Children's Hospital, Sydney, NSW, Australia.; Witting N; Department of Neurology, University Hospital Rigshospitalet, Copenhagen, Denmark.; Vissing J; Department of Neurology, University Hospital Rigshospitalet, Copenhagen, Denmark.; Hanson R; University of Missouri-Kansas City School of Medicine, Kansas City, USA.; Department of Pediatrics, Children's Mercy Hospital, Kansas City, USA.; Coffman KA; Department of Pediatrics, Children's Mercy Hospital, Kansas City, USA.; Division of Neurology, Children's Mercy Hospital, Kansas City, USA.; Hainlen M; Department of Pediatrics, Children's Mercy Hospital, Kansas City, USA.; Division of Neurology, Children's Mercy Hospital, Kansas City, USA.; Parboosingh JS; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.; Carnevale A; Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Yoon G; Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Schnur RE; GeneDx, Gaithersburg, MD, USA.; Boycott KM; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Care4Rare Research Consortium, Ottawa, Canada.; Mah JK; Departments of Pediatrics, Section of Neurology, University of Calgary, Calgary, AB, Canada.; Straub V; John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.; Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Foley AR; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Innes AM; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.; Bönnemann CG; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA. Carsten.bonnemann@nih.gov.; Shutt TE; Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, Canada. timothy.shutt@ucalgary.ca.; Department of Medical Genetics, Alberta Children's Hospital Research Institute, Hotchkiss Brain Institute, University of Calgary, Calgary, Canada. timothy.shutt@ucalgary.ca.

Publisher: Springer Verlag Country of Publication: Germany NLM ID: 0412041 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-0533 (Electronic) Linking ISSN: 00016322 NLM ISO Abbreviation: Acta Neuropathol Subsets: MEDLINE

Gauquelin, L; Cayami, FK; Sztriha, L; Yoon, G; Tran, LT; Guerrero, K; Hocke, F; van Spaendonk, RM; Fung, EL; D'Arrigo, S; Vasco, G; Thiffault, I; Niyazov, DM; Person, R; Lewis, KS; Wassmer, E; Prescott, T; Fallon, P; McEntagart, M; Rankin, J; et al

Publisher: Cambridge University Press ISSN: 0317-1671

Gauquelin, L; Hartley, T; Tarnopolsky, M; Dyment, DA; Brais, B; Geraghty, MT; Tétreault, M; Ahmed, S; Rojas, S; Majewski, J; Bernier, F; Innes, A; Rouleau, G; Suchowersky, O; Boycott, KM; Yoon, G

Publisher: Cambridge University Press ISSN: 0317-1671

Stavropoulos, J; Chung, BH; Marshall, CR; Yoon, G; Scherer, SW; Weksberg, R

American Journal of Medical Genetics Part A. 155:424-429

Buhren, J; Pesudovs, Konrad; Martin, T; Strenger, A; Yoon, G; Kohnen, T

Journal of Cataract and Refractive Surgery. 35:846-855

Hartley T; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Wagner JD; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Warman-Chardon J; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada.; Tétreault M; Department of Human Genetics, McGill University, Montréal, Canada.; Brady L; Department of Pediatrics, McMaster University Medical Centre, Hamilton, Canada.; Baker S; Department of Medicine, McMaster University Medical Centre, Hamilton, Canada.; Tarnopolsky M; Department of Pediatrics, McMaster University Medical Centre, Hamilton, Canada.; Bourque PR; Department of Medicine, University of Ottawa, Ottawa, Canada.; Parboosingh JS; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Canada.; Smith C; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Canada.; McInnes B; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Canada.; Innes AM; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Canada.; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Canada.; Bernier F; Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, Canada.; Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Canada.; Curry CJ; Department of Pediatrics, University of California, San Francisco, California.; Yoon G; Divisions of Neurology and Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Canada.; Horvath GA; Division of Biochemical Diseases, Department of Pediatrics, B.C. Children's Hospital, University of British Columbia, Vancouver, Canada.; Bareke E; Department of Human Genetics, McGill University, Montréal, Canada.; Gillespie M; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Majewski J; Department of Human Genetics, McGill University, Montréal, Canada.; Bulman DE; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Dyment DA; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada.; Boycott KM; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada.

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

Al-Maawali A; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Department of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University, Muscat, Oman.; Yoon G; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Division of Neurology, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Feigenbaum AS; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Division of Genetics, Department of Pediatrics, University of California, San Diego, La Jolla, CA, USA.; Halliday WC; Division of Pathology, DPLM, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Clarke JT; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Branson HM; Division of Paediatric Neuroradiology, The Hospital for Sick Children, University of Toronto, 555 University Avenue, Toronto, M5G 1X8, Ontario, Canada.; Banwell BL; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Chitayat D; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.; Blaser SI; Division of Paediatric Neuroradiology, The Hospital for Sick Children, University of Toronto, 555 University Avenue, Toronto, M5G 1X8, Ontario, Canada. susan.blaser@sickkids.ca.

Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 1302751 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1920 (Electronic) Linking ISSN: 00283940 NLM ISO Abbreviation: Neuroradiology Subsets: MEDLINE

Pope V; Department of Dermatology, Hospital for Sick Children, Toronto, ON, Canada.; Dupuis L; Department of Genetics and Metabolics, Hospital for Sick Children, Toronto, ON, Canada.; Kannu P; Department of Genetics and Metabolics, Hospital for Sick Children, Toronto, ON, Canada.; Mendoza-Londono R; Department of Genetics and Metabolics, Hospital for Sick Children, Toronto, ON, Canada.; Sajic D; Department of Dermatology, Hospital for Sick Children, Toronto, ON, Canada.; So J; University Health Network and Mount Sinai Hospital, The Fred A. Litwin Family Centre in Genetic Medicine, Toronto, ON, Canada.; Centre for Addiction and Mental Health, Toronto, ON, Canada.; University of Toronto, Department of Laboratory Medicine and Pathobiology, Toronto, ON, Canada.; Yoon G; Department of Genetics and Metabolics, Hospital for Sick Children, Toronto, ON, Canada.; Lara-Corrales I; Pediatrics Section of Dermatology, Hospital for Sick Children, Toronto, ON, Canada.; University of Toronto, Toronto, ON, Canada.

Publisher: Oxford University Press Country of Publication: England NLM ID: 0004041 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2133 (Electronic) Linking ISSN: 00070963 NLM ISO Abbreviation: Br J Dermatol Subsets: MEDLINE

Avila M; EA4271 'Génétique des Anomalies du Développement' (GAD), Université de Bourgogne, Dijon, France.; Service de Pédiatrie 1, Centre Hospitalier Universitaire Dijon, Dijon, France.; Dyment DA; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Sagen JV; Hormone Laboratory, Haukeland University Hospital, Bergen, Norway.; KJ Jebsen Center for Diabetes Research, Department of Clinical Science, University of Bergen, Bergen, Norway.; St-Onge J; EA4271 'Génétique des Anomalies du Développement' (GAD), Université de Bourgogne, Dijon, France.; CHU Dijon, Laboratoire de Génétique Moléculaire, Dijon, France.; Moog U; Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany.; Chung BHY; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong - Shenzhen Hospital, Shenzhen, China.; Mo S; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong - Shenzhen Hospital, Shenzhen, China.; Mansour S; SW Thames Regional Genetics Service, St. George's Hospital Medical School, London, SW17 0RE, UK.; Albanese A; Paediatric Endocrine Unit, St George's Hospital, London, UK.; Garcia S; Institute of Medical and Molecular Genetics (INGEMM), La Paz University Hospital, Madrid, Spain.; Instituto de Salud Carlos III, Unit 753, Centro de Investigacion Biomedica en Red de Enfermedades Raras (CIBERER), Madrid, Spain.; Martin DO; Department of Ophthalmology, Hospital Central de la Cruz Roja San Jose y Santa Adela, Madrid, Spain.; Lopez AA; Puerta de Hierro, University Hospital, Madrid, Spain.; Claudi T; Department of Medicine, Bodø, Norway.; König R; Department of Human Genetics, University of Frankfurt, Frankfurt, Germany.; White SM; Victorian Clinical genetics Services, Murdoch Childrens Research institute, Parkville, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, Australia.; Sawyer SL; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.; Bernstein JA; Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CA, USA.; Slattery L; Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CA, USA.; Jobling RK; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Yoon G; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Curry CJ; Genetic Medicine/, University of California, San Francisco, CA, USA.; Merrer ML; Département de Génétique, Hôpital Necker Enfants Malades, Paris, France.; Luyer BL; Service de Pédiatrie, CH Le Havre, Le Havre, France.; Héron D; Département de Génétique et Centre de Référence 'Déficiences intellectuelles de causes rares', Paris, France.; Mathieu-Dramard M; Service de Génétique clinique, Amiens, France.; Bitoun P; Service de Pédiatrie, Bondy, France.; Odent S; Service de Génétique clinique, Rennes, France.; UMR CNRS 6290 IGDR, Universitė Rennes, Rennes, France.; Amiel J; Département de Génétique, Hôpital Necker Enfants Malades, Paris, France.; Kuentz P; EA4271 'Génétique des Anomalies du Développement' (GAD), Université de Bourgogne, Dijon, France.; Thevenon J; EA4271 'Génétique des Anomalies du Développement' (GAD), Université de Bourgogne, Dijon, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs de l'interrégion Est, FHU-TRANSLAD, Dijon, France.; Laville M; Département d'Endocrinologie, Diabétologie et Nutrition, Hospices Civils de Lyon, Centre Hospitalier Lyon-Sud, Pierre-Bénite, France.; Institut National de la Santé et de la Recherche Médicale Unité 1060, Centre Européen pour la nutrition et la Santé, Centre de Recherche en Nutrition Humaine Rhône-Alpes, Université Claude Bernard Lyon, Pierre-Bénite, France.; Reznik Y; Service d'Endocrinologie, Centre Hospitalier Universitaire Côte-de-Nacre, Caen, France.; Fagour C; Département d'Endocrinologie, Hôpital Haut-Lévêque, Centre Hospitalier Universitaire de Bordeaux, Pessac, France.; Nunes ML; Département d'Endocrinologie, Hôpital Haut-Lévêque, Centre Hospitalier Universitaire de Bordeaux, Pessac, France.; Delesalle D; Service de pédiatrie, CH de Valencienne, Valencienne, France.; Manouvrier S; Centre de Référence CLAD NdF - Service de génétique clinique Guy Fontaine, CHRU de Lille - Hôpital Jeanne de Flandre, Lille, France.; Lascols O; INSERM, UMR_S938, Centre de Recherche Saint-Antoine, Paris, France.; UPMC Univ Paris 06, Paris, France.; ICAN, Institute of Cardiometabolism And Nutrition, Groupe Hospitalier Universitaire La Pitié-Salpêtrière, Paris, France.; AP-HP, Hôpital Saint-Antoine, Laboratoire Commun de Biologie et Génétique Moléculaires, Paris, France.; Huet F; EA4271 'Génétique des Anomalies du Développement' (GAD), Université de Bourgogne, Dijon, France.; Service de Pédiatrie 1, Centre Hospitalier Universitaire Dijon, Dijon, France.; Binquet C; Centre d'Investigation Clinique-Epidémiologique Clinique/essais cliniques du CHU de Dijon, Dijon, France.; Faivre L; EA4271 'Génétique des Anomalies du Développement' (GAD), Université de Bourgogne, Dijon, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs de l'interrégion Est, FHU-TRANSLAD, Dijon, France.; Rivière JB; EA4271 'Génétique des Anomalies du Développement' (GAD), Université de Bourgogne, Dijon, France.; CHU Dijon, Laboratoire de Génétique Moléculaire, Dijon, France.; Vigouroux C; INSERM, UMR_S938, Centre de Recherche Saint-Antoine, Paris, France.; UPMC Univ Paris 06, Paris, France.; ICAN, Institute of Cardiometabolism And Nutrition, Groupe Hospitalier Universitaire La Pitié-Salpêtrière, Paris, France.; AP-HP, Hôpital Saint-Antoine, Laboratoire Commun de Biologie et Génétique Moléculaires, Paris, France.; Njølstad PR; Department of Pediatrics, Haukeland, University Hospital, Bergen, Norway.; Innes AM; Department of Medical Genetics, University of Calgary, Calgary, Canada.; Alberta Children's Hospital Research Institute for Child and Maternal Health, University of Calgary, Calgary, Canada.; Thauvin-Robinet C; EA4271 'Génétique des Anomalies du Développement' (GAD), Université de Bourgogne, Dijon, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs de l'interrégion Est, FHU-TRANSLAD, Dijon, 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: PubMed not MEDLINE