부산대학교 도서관

Johnson R; Molecular Cardiology Division, Victor Chang Cardiac Research Institute, 405 Liverpool St, Darlinghurst, NSW 2010, Australia.; School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Kensington, NSW 2052, Australia.; Fletcher RA; The George Institute for Global Health, University of New South Wales, Sydney, NSW, Australia.; Department of Public Health and Primary Care, British Heart Foundation Cardiovascular Epidemiology Unit, University of Cambridge, Cambridge, UK.; Victor Phillip Dahdaleh Heart and Lung Research Institute, University of Cambridge, Cambridge, UK.; Peters S; Department of Cardiology, Royal Melbourne Hospital, Melbourne, VIC, Australia.; Ohanian M; Molecular Cardiology Division, Victor Chang Cardiac Research Institute, 405 Liverpool St, Darlinghurst, NSW 2010, Australia.; Soka M; Molecular Cardiology Division, Victor Chang Cardiac Research Institute, 405 Liverpool St, Darlinghurst, NSW 2010, Australia.; Smolnikov A; School of Biotechnology and Biomolecular Sciences, Faculty of Science, UNSW Sydney, Sydney, NSW, Australia.; Abihider KE; Division of Clinical Genetics, Department of Obstetrics and Gynecology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.; Ackerman MJ; Department of Cardiovascular Medicine, Division of Heart Rhythm Services, Windland Smith Rice Genetic Heart Rhythm Clinic, Mayo Clinic, Rochester, MN, USA.; Department of Pediatric and Adolescent Medicine, Division of Pediatric Cardiology, Mayo Clinic, Rochester, MN, USA.; Department of Molecular Pharmacology and Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN, USA.; Ader F; Department of Cardiogenetic and Myogenetic Molecular and Cellular, Metabolic Biochemistry, AP-HP Sorbonne Université, Pitié Salpêtrière Hospital, Paris, France.; Akhtar MM; Centre for Heart Muscle Disease, Institute of Cardiovascular Science, University College London, London, UK.; Cardiology Department, Royal Brompton & Harefield Hospitals, Guy's and St. Thomas' NHS Foundation Trust, London, UK.; Amin AS; Department of Clinical Cardiology, Heart Center, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Ashley EA; Department of Medicine, Stanford University, Stanford, CA, USA.; Department of Genetics, Stanford University, Stanford, CA, USA.; Department of Biomedical Data Science, Stanford University, Stanford, CA, USA.; Atherton JJ; Department of Cardiology, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.; Faculty of Medicine, University of Queensland, Brisbane, QLD, Australia.; Austin R; Genetic Health Queensland Service, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.; Australian Genomics, Melbourne, VIC, Australia.; Baas AF; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Bagnall RD; Bioinformatics and Molecular Genetics Group, Centenary Institute, University of Sydney, Sydney, NSW, Australia.; Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.; Ross SB; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.; Blouin JL; Department of Diagnostics, Service of Genetic Medicine, University Hospitals of Geneva, Geneva, Switzerland.; Brown EE; Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA.; Bundgaard H; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.; Cannie D; Centre for Heart Muscle Disease, Institute of Cardiovascular Science, University College London, London, UK.; Department of Inherited Cardiovascular Diseases, Barts Heart Centre, St Bartholomew's Hospital, London, UK.; Chmielewski P; Unit for Screening Studies in Inherited Cardiovascular Diseases, National Institute of Cardiology, Warsaw, Poland.; Correnti G; Adult Genetics Unit, Royal Adelaide Hospital, Adelaide, SA, Australia.; Crespo-Leiro MG; Heart Failure and Heart Transplant Unit, Complexo Hospitalario Universitario a Coruña, Centro de Investigación Biomédica en Red (CIBERCV), Instituto de Investigación Biomédica de A Coruña (INIBIC), Universidade da Coruña, La Coruña, Spain.; Dal Ferro M; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiothoracovascular, Azienda Sanitaria Universitaria Integrata, Trieste, Italy.; Department of Medicine, University of Trieste, Trieste, Italy.; Dellefave-Castillo LM; Center for Genetic Medicine, Northwestern University, Evanston, IL, USA.; Center for Genetic Medicine, Bluhm Cardiovascular Institute, Chicago, IL, USA.; Dominguez F; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, Hospital Universitario Puerta de Hierro, Instituto Investigación Sanitaria Puerta de Hierro-Segovia de Arana, CIBERCV, Madrid, Spain.; Dooijes D; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Dybro AM; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.; Ed Demri Y; Cardiology Department, AP-HP, Cochin Hospital, Paris, France.; El Hachmi M; Département de Génétique, AP-HP, Hôpital Européen Georges Pompidou, Service de Médecine Génomique des Maladies Rares, Paris, France.; Department of Molecular Medicine, Sapienza University of Rome, Rome, Italy.; Escobar-Lopez L; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, Hospital Universitario Puerta de Hierro, Instituto Investigación Sanitaria Puerta de Hierro-Segovia de Arana, CIBERCV, Madrid, Spain.; Foye SJ; Team Titin, Inc . Pine Brook, NJ, USA.; Franaszczyk M; Department of Medical Biology, National Institute of Cardiology, Warsaw, Poland.; Department of Medical Genetics, Warsaw Medical University, Warsaw, Poland.; Gigli M; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiothoracovascular, Azienda Sanitaria Universitaria Integrata, Trieste, Italy.; Department of Medicine, University of Trieste, Trieste, Italy.; Lopez EG; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, Hospital Universitario Puerta de Hierro, Instituto Investigación Sanitaria Puerta de Hierro-Segovia de Arana, CIBERCV, Madrid, Spain.; Goudal A; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Service de Genetique Medicale, Centre Hospitalier Universitaire de Nantes, Nantes, France.; Graw S; Cardiovascular Institute and Adult Medical Genetics Program, University of Colorado, Cardiovascular Institute, Aurora, CO, USA.; Guipponi M; Department of Diagnostics, Service of Genetic Medicine, University Hospitals of Geneva, Geneva, Switzerland.; Haan E; Faculty of Health and Medical Sciences, University of Adelaide, Adelaide, SA, Australia.; Haas J; Department of Cardiology, Pneumology and Angiology, Heidelberg University Hospital, Heidelberg, Germany.; Informatics for Life, Heidelberg, Germany.; DZHK (German Center for Cardiovascular Research), Partner Site Heidelberg/Mannheim, Heidelberg, Germany.; Hammersley DJ; Cardiology Department, Royal Brompton & Harefield Hospitals, Guy's and St. Thomas' NHS Foundation Trust, London, UK.; National Heart and Lung Institute, Imperial College, London, UK.; Hansen FG; Department of Cardiology, Odense University Hospital, Odense, Denmark.; Hayward CS; School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Kensington, NSW 2052, Australia.; Heart Transplantation Division, Victor Chang Cardiac Research Institute, Sydney, NSW, Australia.; Cardiology Department, St Vincent's Hospital Sydney, 390 Victoria St, Darlinghurst, NSW 2010, Australia.; Hey TM; Department of Cardiology, Odense University Hospital, Odense, Denmark.; Heymans S; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiovascular Sciences, Centre for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.; Department of Cardiology, Maastricht University, Cardiovascular Research Institute Maastricht, Maastricht, The Netherlands.; Ho CY; Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.; Houweling AC; Department of Human Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.; Ingles J; School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Kensington, NSW 2052, Australia.; Genomics and Inherited Disease Program, Garvan Institute of Medical Research, Sydney, NSW, Australia.; Ingrey A; Hunter Genetics, Hunter New England Local Health District, Newcastle, NSW, Australia.; Jabbour A; School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Kensington, NSW 2052, Australia.; Heart Transplantation Division, Victor Chang Cardiac Research Institute, Sydney, NSW, Australia.; Cardiology Department, St Vincent's Hospital Sydney, 390 Victoria St, Darlinghurst, NSW 2010, Australia.; James PA; Genomic Medicine, Royal Melbourne Hospital, Melbourne, VIC, Australia.; Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, VIC, Australia.; Jansweijer JA; Department of Clinical and Experimental Cardiology, Amsterdam University Medical Centre, Amsterdam, The Netherlands.; Department of Cardiology, Haga Teaching Hospital, The Hague, The Netherlands.; Jongbloed JDH; Department of Genetics, University Medical Center Groningen, Groningen, The Netherlands.; Keogh AM; School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Kensington, NSW 2052, Australia.; Heart Transplantation Division, Victor Chang Cardiac Research Institute, Sydney, NSW, Australia.; Cardiology Department, St Vincent's Hospital Sydney, 390 Victoria St, Darlinghurst, NSW 2010, Australia.; Larrañaga-Moreira JM; Unidad de Cardiopatías Familiares, INIBIC, Complexo Hospitalario Universitario de A Coruña, Servizo Galego de Saúde, Universidade da Coruña, A Coruña, Spain.; Lekanne Deprez RH; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Human Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.; Macciocca I; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.; Macdonald PS; School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Kensington, NSW 2052, Australia.; Heart Transplantation Division, Victor Chang Cardiac Research Institute, Sydney, NSW, Australia.; Cardiology Department, St Vincent's Hospital Sydney, 390 Victoria St, Darlinghurst, NSW 2010, Australia.; Mansencal N; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Emergency Medicine, AP-HP, Hôpital Ambroise Paré, Boulogne-Billancourt, France.; Mansour J; Tasmanian Clinical Genetics Service and Tasmanian Health Service, Hobart, TAS, Australia.; Martinez-Veira C; Unidad de Cardiopatías Familiares, CIBERCV, Madrid, Spain.; McDonough B; Department of Genetics, Harvard Medical School, Boston, MA, USA.; McGaughran J; Genetic Health Queensland Service, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.; School of Medicine, The University of Queensland, Brisbane, QLD, Australia.; Medo K; Cardiovascular Institute and Adult Medical Genetics Program, University of Colorado, Cardiovascular Institute, Aurora, CO, USA.; Merlo M; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiothoracovascular, Azienda Sanitaria Universitaria Integrata, Trieste, Italy.; Department of Medicine, University of Trieste, Trieste, Italy.; Michalak E; Unit for Screening Studies in Inherited Cardiovascular Diseases, National Institute of Cardiology, Warsaw, Poland.; Monserrat L; Department of Cardiology, Health in Code, A Coruña, Spain.; Mountain H; Genetic Services of Western Australia, Perth, WA, Australia.; Genetic Counselling Department, Graduate School of Health, University of Technology Sydney, Sydney, NSW, Australia.; Muller SA; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.; Murphy AM; Division of Pediatric Cardiology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.; Murray B; Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA.; Oates EC; School of Biotechnology and Biomolecular Sciences, Faculty of Science, UNSW Sydney, Sydney, NSW, Australia.; Department of Neurology, Sydney Children's Hospital, Sydney, NSW, Australia.; Ormondroyd E; Radcliffe Department of Medicine, University of Oxford, Oxford, UK.; NIHR Oxford Biomedical Research Centre, Oxford, UK.; Pachter N; Genetic Services of Western Australia, Perth, WA, Australia.; Genetic Services Department, King Edward Memorial Hospital, Perth, WA, Australia.; School of Medicine, University of Western Australia, Perth, WA, Australia.; Paldino A; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiothoracovascular, Azienda Sanitaria Universitaria Integrata, Trieste, Italy.; Department of Medicine, University of Trieste, Trieste, Italy.; Palmyre A; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Genetics and Referral Center for Hereditary Cardiac Diseases, AP-HP, Hôpital Ambroise Paré, Boulogne-Billancourt, France.; Pereira NL; Department of Cardiovascular Medicine, Division of Heart Rhythm Services, Windland Smith Rice Genetic Heart Rhythm Clinic, Mayo Clinic, Rochester, MN, USA.; Department of Molecular Pharmacology and Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN, USA.; Picard KC; Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.; Poplawski N; Adult Genetics Unit, Royal Adelaide Hospital, Adelaide, SA, Australia.; Discipline of Paediatrics, Adelaide Medical School, University of Adelaide, Adelaide, SA, Australia.; Prasad S; National Heart and Lung Institute, Imperial College, London, UK.; Proukhnitzky J; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Genetics and Cardiology Department, Sorbonne Université, AP-HP, INSERM UMRS_1166, IHU-ICAN, Hôpital Pitié-Salpêtrière, Paris, France.; Pruny JF; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Sorbonne Université, Centre de Référence pour les Maladies Cardiaques Héréditaires ou rares, AP-HP, INSERM UMRS_1166, IHU-ICAN, Hôpital Pitié-Salpêtrière, Paris, France.; Reant P; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Service de Cardiologie, Centre Hospitalier Universitaire de Bordeaux, Université de Bordeaux, CIC 1401, Bordeaux, France.; French Reference Center in Inherited Cardiomyopathies, ERN GUARD-Heart, Bordeaux, France.; Richard P; Department of Cardiogenetic and Myogenetic Molecular and Cellular, Metabolic Biochemistry, AP-HP Sorbonne Université, Pitié Salpêtrière Hospital, Paris, France.; Ronan A; Genetics Unit, Newcastle Medical Genetics, Newcastle, NSW, Australia.; School of Medicine and Public Health, College of Health, Medicine and Wellbeing, University of Newcastle, Newcastle, NSW, Australia.; Sedaghat-Hamedani F; Department of Cardiology, Pneumology and Angiology, Heidelberg University Hospital, Heidelberg, Germany.; Informatics for Life, Heidelberg, Germany.; DZHK (German Center for Cardiovascular Research), Partner Site Heidelberg/Mannheim, Heidelberg, Germany.; Semsarian C; Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.; Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, University of Sydney, Sydney, NSW, Australia.; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.; Storm G; Cardiovascular Institute and Adult Medical Genetics Program, University of Colorado, Cardiovascular Institute, Aurora, CO, USA.; Stroeks S; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, Maastricht University, Cardiovascular Research Institute Maastricht, Maastricht, The Netherlands.; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Syrris P; Centre for Heart Muscle Disease, Institute of Cardiovascular Science, University College London, London, UK.; Taylor MRG; Cardiovascular Institute and Adult Medical Genetics Program, University of Colorado, Cardiovascular Institute, Aurora, CO, USA.; Thomson K; Radcliffe Department of Medicine, University of Oxford, Oxford, UK.; Oxford Regional Genetics Laboratories, Churchill Hospital, Oxford, UK.; Thompson T; Genomic Medicine, Royal Melbourne Hospital, Melbourne, VIC, Australia.; Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, VIC, Australia.; van Tintelen JP; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Vissing CR; Department of Cardiology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.; Cardiology Department, Hvidovre Hospital, Copenhagen University Hospital, Copenhagen, Denmark.; Waddell-Smith KE; Adult Genetics Unit, Royal Adelaide Hospital, Adelaide, SA, Australia.; Wallis M; Tasmanian Clinical Genetics Service and Tasmanian Health Service, Hobart, TAS, Australia.; School of Medicine and Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.; Zentner D; Department of Cardiology, Royal Melbourne Hospital, Melbourne, VIC, Australia.; Genomic Medicine, Royal Melbourne Hospital, Melbourne, VIC, Australia.; Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, VIC, Australia.; Arnott C; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.; Cardiovascular Program, The George Institute for Global Health, UNSW Sydney, Sydney, NSW, Australia.; Marian AJ; Center for Cardiovascular Genetic Research, Institute of Molecular Medicine, University of Texas Health Science Center, Houston, TX, USA.; Oh J; Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Korea.; Fokstuen S; Department of Diagnostics, Service of Genetic Medicine, University Hospitals of Geneva, Geneva, Switzerland.; James CA; Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA.; Barriales-Villa R; Inherited Cardiovascular Disease Unit, Complexo Hospitalario Universitario A Coruña, A Coruña, Galicia, Spain.; Meder B; Department of Cardiology, Pneumology and Angiology, Heidelberg University Hospital, Heidelberg, Germany.; Informatics for Life, Heidelberg, Germany.; DZHK (German Center for Cardiovascular Research), Partner Site Heidelberg/Mannheim, Heidelberg, Germany.; Wahbi K; Cardiology Department, AP-HP, Cochin Hospital, Paris, France.; Faculté de Médecine, Université Paris-Cité, Paris, France.; Giudicessi JR; Department of Cardiovascular Medicine, Division of Heart Rhythm Services, Windland Smith Rice Genetic Heart Rhythm Clinic, Mayo Clinic, Rochester, MN, USA.; Department of Molecular Pharmacology and Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN, USA.; Parikh VN; Department of Medicine, Stanford Center for Inherited Cardiovascular Disease, Stanford, CA, USA.; Ware JS; Cardiology Department, Royal Brompton & Harefield Hospitals, Guy's and St. Thomas' NHS Foundation Trust, London, UK.; Cardiovascular and Genomic Medicine, National Heart and Lung Institute and MRC London Institute of Medical Sciences, Imperial College London, London, UK.; Piriou N; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Centre de Référence Cardiomyopathies, L'institut du Thorax, Nantes Université, Nantes, France.; Rooryck C; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Service de Génétique Médicale, CHU Bordeaux, Bordeaux, France.; Maladies Rares: Génétique et Métabolisme, Université de Bordeaux, INSERMU1211, Bordeaux, France.; Lakdawala NK; Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.; Department of Medicine, Harvard Medical School, Boston, MA, USA.; Mestroni L; Cardiovascular Institute and Adult Medical Genetics Program, University of Colorado, Cardiovascular Institute, Aurora, CO, USA.; Sinagra G; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiothoracovascular, Azienda Sanitaria Universitaria Integrata, Trieste, Italy.; Department of Medicine, University of Trieste, Trieste, Italy.; Elliott PM; Centre for Heart Muscle Disease, Institute of Cardiovascular Science, University College London, London, UK.; Department of Inherited Cardiovascular Diseases, Barts Heart Centre, St Bartholomew's Hospital, London, UK.; Watkins H; Radcliffe Department of Medicine, University of Oxford, Oxford, UK.; McNally EM; Center for Genetic Medicine, Northwestern University, Evanston, IL, USA.; Center for Genetic Medicine, Bluhm Cardiovascular Institute, Chicago, IL, USA.; Charron P; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Genetics and Referral Center for Hereditary Cardiac Diseases, AP-HP, Hôpital Ambroise Paré, Boulogne-Billancourt, France.; Sorbonne Université, Centre de Référence pour les Maladies Cardiaques Héréditaires ou rares, AP-HP, INSERM UMRS_1166, IHU-ICAN, Hôpital Pitié-Salpêtrière, Paris, France.; van Spaendonck-Zwarts KY; Genetic Health Queensland Service, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.; Department of Human Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.; Department of Genetics, University Medical Center Groningen, Groningen, The Netherlands.; Garcia-Pavia P; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, Hospital Universitario Puerta de Hierro, Instituto Investigación Sanitaria Puerta de Hierro-Segovia de Arana, CIBERCV, Madrid, Spain.; Centro Nacional de Investigaciones Cardiovasculares, Madrid, Spain.; Peña-Peña ML; Department of Cardiology, Virgen del Rocio University Hospital, Seville, Spain.; Mogensen J; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, Aalborg University Hospital, Aalborg, Denmark.; Christensen AH; Department of Cardiology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.; Bilińska ZT; Unit for Screening Studies in Inherited Cardiovascular Diseases, National Institute of Cardiology, Warsaw, Poland.; Rasmussen TB; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.; Seidman JG; Department of Genetics, Harvard Medical School, Boston, MA, USA.; Seidman CE; Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.; Department of Genetics, Harvard Medical School, Boston, MA, USA.; Te Riele ASJM; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.; Verdonschot JAJ; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Cardiology, Maastricht University, Cardiovascular Research Institute Maastricht, Maastricht, The Netherlands.; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Pinto YM; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart (ERN GUARD-Heart), Amsterdam, The Netherlands.; Department of Clinical Cardiology and Experimental Cardiology, University of Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands.; Christiaans I; Department of Genetics, University Medical Center Groningen, Groningen, The Netherlands.; Fatkin D; Molecular Cardiology Division, Victor Chang Cardiac Research Institute, 405 Liverpool St, Darlinghurst, NSW 2010, Australia.; School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Kensington, NSW 2052, Australia.; Cardiology Department, St Vincent's Hospital Sydney, 390 Victoria St, Darlinghurst, NSW 2010, Australia.

Publisher: Oxford University Press Country of Publication: England NLM ID: 8006263 Publication Model: Print Cited Medium: Internet ISSN: 1522-9645 (Electronic) Linking ISSN: 0195668X NLM ISO Abbreviation: Eur Heart J Subsets: MEDLINE

Zgheib O; Division of Genetic Medicine, Department of Diagnostics, Geneva University Hospitals, Switzerland.; Jacques L; Division of General Pediatrics, Department of Pediatrics, Gynecology and Obstetrics, Geneva University Hospitals, Switzerland.; Frizon L; Division of General Pediatrics, Department of Pediatrics, Gynecology and Obstetrics, Geneva University Hospitals, Switzerland.; Windisch G; Division of General Pediatrics, Department of Pediatrics, Gynecology and Obstetrics, Geneva University Hospitals, Switzerland.; Fokstuen S; Division of Genetic Medicine, Department of Diagnostics, Geneva University Hospitals, Switzerland.

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

Zgheib O; Division of Medical Genetics, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.; Rio Frio T; Molecular Diagnostics Laboratory, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.; Pellegrinelli JM; Division of Fetal Medicine, Department of Obstetrics, Gynecology and Pediatrics, Geneva University Hospitals, Geneva, Switzerland.; Gimelli S; Cytogenetics Laboratory, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.; Marconi C; Cytogenetics Laboratory, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.; Le Mercier D; Division of Fetal Medicine, Department of Obstetrics, Gynecology and Pediatrics, Geneva University Hospitals, Geneva, Switzerland.; Rebollo Polo M; Division of Radiology, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.; Habre C; Division of Radiology, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.; Fluss J; Division of Neuropediatrics, Department of Obstetrics, Gynecology and Pediatrics, Geneva University Hospitals, Geneva, Switzerland.; Ha-Vinh Leuchter R; Division of Child Development, Department of Obstetrics, Gynecology and Pediatrics, Geneva University Hospitals, Geneva, Switzerland.; Abramowicz M; Division of Medical Genetics, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.; Giannini R; Division of Medical Genetics, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.; Fokstuen S; Division of Medical Genetics, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.

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

Zgheib O; Service de Médecine Génétique, Hôpitaux Universitaire Genève, Genève, Switzerland.; Rio-Frio T; Service de Médecine Génétique, Hôpitaux Universitaire Genève, Genève, Switzerland.; Département de Médecine Génétique et Développement, Faculté de Médecine, Université de Genève, Genève, Switzerland.; Guipponi M; Service de Médecine Génétique, Hôpitaux Universitaire Genève, Genève, Switzerland.; Département de Médecine Génétique et Développement, Faculté de Médecine, Université de Genève, Genève, Switzerland.; Nouspikel T; Service de Médecine Génétique, Hôpitaux Universitaire Genève, Genève, Switzerland.; Département de Médecine Génétique et Développement, Faculté de Médecine, Université de Genève, Genève, Switzerland.; Fokstuen S; Service de Médecine Génétique, Hôpitaux Universitaire Genève, Genève, Switzerland.; Universitäres Herzzentrum Zürich, Klinik für Kardiologie Universitätsspital Zürich, Zürich, Switzerland.; Abramowicz M; Service de Médecine Génétique, Hôpitaux Universitaire Genève, Genève, Switzerland.; Département de Médecine Génétique et Développement, Faculté de Médecine, Université de Genève, Genève, Switzerland.; Khau Van Kien P; Service de Médecine Génétique, Hôpitaux Universitaire Genève, Genève, Switzerland.; Département de Médecine Génétique et Développement, Faculté de Médecine, Université de Genève, Genève, Switzerland.

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

Bahadoer, Renu R, MD; Dijkstra, Esmée A, MD; van Etten, Boudewijn, MD; Marijnen, Corrie A M, Prof; Putter, Hein, Prof; Kranenbarg, Elma Meershoek-Klein, MSc; Roodvoets, Annet G H, MSc; Nagtegaal, Iris D, Prof; Beets-Tan, Regina G H, Prof; Blomqvist, Lennart K, Prof; Fokstuen, Tone, MD; ten Tije, Albert J, MD; Capdevila, Jaume, MD; Hendriks, Mathijs P, MD; Edhemovic, Ibrahim, MD; Cervantes, Andrés, Prof; Nilsson, Per J, MD; Glimelius, Bengt, Prof; van de Velde, Cornelis J H, Prof; Hospers, Geke A P, Prof; Østergaard, L.; Svendsen Jensen, F.; Pfeiffer, P.; Jensen, K.E.J.; Hendriks, M.P.; Schreurs, W.H.; Knol, H.P.; van der Vliet, J.J.; Tuynman, J.B.; Bruynzeel, A.M.E.; Kerver, E.D.; Festen, S.; van Leerdam, M.E.; Beets, G.L.; Dewit, L.G.H.; Punt, C.J.A.; Tanis, P.J.; Geijsen, E.D.; Nieboer, P.; Bleeker, W.A.; Ten Tije, A.J.; Crolla, R.M.P.H.; van de Luijtgaarden, A.C.M.; Dekker, J.W.T.; Immink, J.M.; Jeurissen, F.J.F.; Marinelli, A.W.K.S.; Ceha, H.M.; Stam, T.C.; Quarles an Ufford, P.; Steup, W.H.; Imholz, A.L.T.; Bosker, R.J.I.; Bekker, J.H.M.; Creemers, G.J.; Nieuwenhuijzen, G.A.P.; van den Berg, H.; van der Deure, W.M.; Schmitz, R.F.; van Rooijen, J.M.; Olieman, A.F.T.; van den Bergh, A.C.M.; de Groot, D.J.A.; Havenga, K.; Beukema, J.C.; de Boer, J.; Veldman, P.H.J.M.; Siemerink, E.J.M.; Vanstiphout, J.W.P.; de Valk, B.; Eijsbouts, Q.A.J.; Polée, M.B.; Hoff, C.; Slot, A.; Kapiteijn, H.W.; Peeters, K.C.M.J.; Peters, F.P.; Nijenhuis, P.A.; Radema, S.A.; de Wilt, H.; Braam, P.; Veldhuis, G.J.; Hess, D.; Rozema, T.; Reerink, O.; Ten Bokkel Huinink, D.; Pronk, A.; Vos, J.; Tascilar, M.; Patijn, G.A.; Kersten, C.; Mjåland, O.; Grønlie Guren, M.; Nesbakken, A.N.; Benedik, J.; Edhemovic, I.; Velenik, V.; Capdevila, J.; Espin, E.; Salazar, R.; Biondo, S.; Pachón, V.; die Trill, J.; Aparicio, J.; Garcia Granero, E.; Safont, M.J.; Bernal, J.C.; Cervantes, A.; Espí Macías, A.; Malmberg, L.; Svaninger, G.; Hörberg, H.; Dafnis, G.; Berglund, A.; Österlund, L.; Kovacs, K.; Hol, J.; Ottosson, S.; Carlsson, G.; Bratthäll, C.; Assarsson, J.; Lödén, B.L.; Hede, P.; Verbiené, I.; Hallböök, O.; Johnsson, A.; Lydrup, M.L.; Villmann, K.; Matthiessen, P.; Svensson, J.H.; Haux, J.; Skullman, S.; Fokstuen, T.; Holm, T.; Flygare, P.; Walldén, M.; Lindh, B.; Lundberg, O.; Radu, C.; Påhlman, L.; Piwowar, A.; Smedh, K.; Palenius, U.; Jangmalm, S.; Parinkh, P.; Kim, H.; Silviera, M.L.

The Lancet Oncology. 22(1):29-42

Varvagiannis, K; Hanquinet, S; Billieux, M H; De Luca, R; Rimensberger, P; Lidgren, M; Guipponi, M; Makrythanasis, P; Blouin, J L; Antonarakis, S E; Steinfeld, R; Kern, I; Poretti, A; Fluss, J; Fokstuen, S

Neuropediatrics, Vol. 49, No 2 (2018) pp. 150-153

Pierce, Sarah B.; Spurrell, Cailyn H.; Mandell, Jessica B.; Lee, Ming K.; Zeligson, Sharon; Bereman, Michael S.; Stray, Sunday M.; Fokstuen, Siv; MacCoss, Michael J.; Levy-Lahad, Ephrat; King, Mary-Claire; Motulsky, Arno G.

Proceedings of the National Academy of Sciences of the United States of America, 2011 Nov 01. 108(45), 18313-18317.

Massie E; Cardiology Service, University Hospital of Geneva, Rue Gabrielle Perret-Gentil 4, 1205 Geneva, Switzerland.; Dominati A; Division of Immunology and Allergy, Department of Medicine, University Hospitals of Geneva, Geneva, Switzerland.; Suchet S; Service of Genetic Medicine, University Hospital of Geneva, Geneva, Switzerland.; Carballo D; Cardiology Service, University Hospital of Geneva, Rue Gabrielle Perret-Gentil 4, 1205 Geneva, Switzerland.; Hervier E; Cardiology Service, University Hospital of Geneva, Rue Gabrielle Perret-Gentil 4, 1205 Geneva, Switzerland.; Fokstuen S; Service of Genetic Medicine, University Hospital of Geneva, Geneva, Switzerland.; Seebach JD; Division of Immunology and Allergy, Department of Medicine, University Hospitals of Geneva, Geneva, Switzerland.; Meyer P; Cardiology Service, University Hospital of Geneva, Rue Gabrielle Perret-Gentil 4, 1205 Geneva, Switzerland.

Publisher: Oxford University Press Country of Publication: England NLM ID: 101730741 Publication Model: eCollection Cited Medium: Internet ISSN: 2514-2119 (Electronic) Linking ISSN: 25142119 NLM ISO Abbreviation: Eur Heart J Case Rep Subsets: PubMed not MEDLINE

Zgheib O; Division of Genetic Medicine, Department of Diagnostics, Geneva University Hospitals, Geneva, Switzerland.; Trombetti A; Division of Bone Diseases, Department of Medicine, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.; Juillerat A; Division of Internal Medicine, Department of Medicine, Geneva University Hospitals, Geneva, Switzerland.; Fokstuen S; Division of Genetic Medicine, Department of Diagnostics, Geneva University Hospitals, Geneva, Switzerland.

Publisher: SAGE Publications Inc Country of Publication: United States NLM ID: 101691975 Publication Model: eCollection Cited Medium: Internet ISSN: 2329-048X (Electronic) Linking ISSN: 2329048X NLM ISO Abbreviation: Child Neurol Open Subsets: PubMed not MEDLINE

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Human Mutation, Vol. 35, No 10 (2014) pp. 1203-10
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In Journal de Gynecologie Obstetrique et Biologie de la Reproduction April 2013 42(2):159-165

Mogensen J; van Tintelen JP; Fokstuen S; Elliott P; van Langen IM; Meder B; Richard P; Syrris P; Caforio A; Adler Y; Anastasakis A; Gimeno JR; Klingel K; Linhart A; Imazio M; Pinto Y; Newbery R; Schmidtke J; Charron P.

Mogensen, J, van Tintelen, J P, Fokstuen, S, Elliott, P, van Langen, I M, Meder, B, Richard, P, Syrris, P, Caforio, A L P, Adler, Y, Anastasakis, A, Gimeno, J R, Klingel, K, Linhart, A, Imazio, M, Pinto, Y, Newbery, R, Schmidtke, J & Charron, P 2015, ' The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions : a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the European Society of Human Genetics ', European Heart Journal, vol. 36, no. 22, pp. 1367-1370 . https://doi.org/10.1093/eurheartj/ehv122

Fokstuen S; Genetic Medicine, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.; Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.; Quteineh L; Genetic Medicine, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.; Schwitzgebel VM; Pediatric Endocrine and Diabetes Unit, Department of Pediatrics, Gynecology and Obstetrics, Geneva University Hospitals, Geneva, Switzerland.; Diabetes Center of the Faculty of Medicine, University of Geneva, Geneva, Switzerland.; Köhler-Ballan B; Department of Infectious Disease, Geneva University Hospitals, Geneva, Switzerland.; Blouin JL; Genetic Medicine, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.; Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.; Abramowicz M; Genetic Medicine, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.; Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.; Nouspikel T; Genetic Medicine, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.; Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.

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

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Hamamy, H, Antonarakis, S E, Cavalli-Sforza, L L, Temtamy, S, Romeo, G, ten Kate, L P, Bennett, R L, Shaw, A, Megarbane, A, van Duijn, C, Bathija, H, Fokstuen, S, Engel, E, Zlotogora, J, Dermitzakis, E, Bottani, A, Dahoun, S, Morris, M A, Arsenault, S, Aglan, M S, Ajaz, M, Alkalamchi, A, Alnaqeb, D, Alwasiyah, M K, Anwer, N, Awwad, R, Bonnefin, M, Corry, P, Gwanmesia, L, Karbani, G A, Mostafavi, M, Pippucci, T, Ranza-Boscardin, E, Reversade, B, Sharif, S M, Teeuw, M E & Bittles, A H 2011, 'Consanguineous marriages, pearls and perils: Geneva international consanguinity workshop report', Genetics in Medicine, vol. 13, no. 9, pp. 841-847. https://doi.org/10.1097/GIM.0b013e318217477f
Genetics in Medicine, Vol. 13, No 9 (2011) pp. 841-7

Fokstuen, S; Arbenz, U; Artan, S; Dutly, Fabrizio; Bauersfeld, U; Brecevic, L; Fasnacht, M; Röthlisberger, Benno; Schinzel, Albert

Clinical Genetics. 53:63-69

Fokstuen S; Munoz A; MELACINI, PAOLA; ILICETO, SABINO; Perrot A; Ozcelik C; Jeanrenaud X; Rieubland C; Farr M; Faber L; Sigwart U; Mach F; Lerch R; Antonarakis SE; Blouin JL

Journal of Medical Genetics, Vol. 48, No 8 (2011) pp. 572-6
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Annals of Oncology. 21(1):87-91

Marconi C; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Lemmens L; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Masclaux F; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Mattioli F; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Fluss J; Pediatric Specialties division, Department of Women, Children and Adolescents, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Extermann P; Prenatal Ultrasonography, Dianecho, Genève (CH), Switzerland.; Mendez P; Obstetrics and Gynecology, Centre Médical Eaux-Vives, Genève (CH), Switzerland.; Leuchter RH; Pediatric Specialties division, Department of Women, Children and Adolescents, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Stathaki E; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Laurent S; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Hammar E; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Vannier A; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Varvagiannis K; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Guipponi M; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Department of Genetic Medicine and Development, School of Medicine, University of Geneva, Genève (CH), Switzerland.; Sloan-Bena F; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Department of Genetic Medicine and Development, School of Medicine, University of Geneva, Genève (CH), Switzerland.; Blouin JL; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Department of Genetic Medicine and Development, School of Medicine, University of Geneva, Genève (CH), Switzerland.; Abramowicz M; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Department of Genetic Medicine and Development, School of Medicine, University of Geneva, Genève (CH), Switzerland.; Fokstuen S; Genetic Medicine division, Diagnostic Department, Hôpitaux Universitaires de Genève, Genève (CH), Switzerland.; Department of Genetic Medicine and Development, School of Medicine, University of Geneva, Genève (CH), Switzerland.

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

Fokstuen, T; Rabo, YB; Zhou, JN; Karlson, J; Platz, A; Shoshan, MC; Hansson, J; Linder, S

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Human Genomics. June 28, 2016, Vol. 10 Issue 1