부산대학교 도서관

van der Smagt JJ; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; Lampri AP; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; de Lange I; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; Alders M; Amsterdam UMC, Department of Human Genetics, Genome Diagnostics Laboratory, Amsterdam Reproduction & Development, University of Amsterdam, Amsterdam, the Netherlands.; Houben ML; Department of Pediatrics, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, the Netherlands.; Koudijs MJ; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; van Jaarsveld RH; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands. Electronic address: r.h.vanjaarsveld@umcutrecht.nl.

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

D'Incal CP; Cognitive Genetics (CONGET), Centre for Medical Genetics (CMG), Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium Department of Medical Genetics, Antwerp, Belgium.; Protein Chemistry, Proteomics and Epigenetic Signaling (PPES), Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.; Annear DJ; Cognitive Genetics (CONGET), Centre for Medical Genetics (CMG), Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium Department of Medical Genetics, Antwerp, Belgium.; Elinck E; Cognitive Genetics (CONGET), Centre for Medical Genetics (CMG), Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium Department of Medical Genetics, Antwerp, Belgium.; van der Smagt JJ; Division of Laboratories, Pharmacy and Biomedical Genetics, Section Clinical Genetics, University Medical Center Utrecht, the Netherlands and Rijksuniversiteit Utrecht, Utrecht, the Netherlands.; Alders M; Department of Human Genetics, Amsterdam Reproduction & Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Dingemans AJM; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.; Department of Artificial Intelligence, Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.; Mateiu L; Cognitive Genetics (CONGET), Centre for Medical Genetics (CMG), Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium Department of Medical Genetics, Antwerp, Belgium.; de Vries BBA; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.; Vanden Berghe W; Protein Chemistry, Proteomics and Epigenetic Signaling (PPES), Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium. wim.vandenberghe@uantwerpen.be.; Kooy RF; Cognitive Genetics (CONGET), Centre for Medical Genetics (CMG), Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium Department of Medical Genetics, Antwerp, Belgium. frank.kooy@uantwerpen.be.

Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Sewani S; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Azamian MS; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Mendelsohn BA; Department of Medical Genetics, Kaiser Permanente Oakland Medical Center, Oakland, California, USA.; Mau-Them FT; UF6254 Innovation en Diagnostic Genomique des Maladies Rares, Dijon, France.; Équipe Génétique des Anomalies du Développement (GAD), Dijon, France.; Réda M; Department of Medical Oncology, Georges François Leclerc Cancer Center - UNICANCER, Dijon, France.; Platform of Transfer in Cancer Biology, Georges François Leclerc Cancer Center - UNICANCER, Dijon, France.; Université Bourgogne Franche-Comté, Dijon, France.; Genomic and Immunotherapy Medical Institute, Dijon, France.; Nambot S; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, Dijon, France.; Centre de Référence Maladies Rares 'Anomalies du Développement et Syndromes Malformatifs', Centre de Génétique, FHU-TRANSLAD, Dijon, France.; Isidor B; Centre Hospitalier Universitaire de Nantes, Service de Génétique Médicale, Nantes, France.; INSERM, CNRS, UNIV Nantes, l'institut du thorax, Nantes, France.; van der Smagt JJ; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Shen JJ; Division of Genomic Medicine, Department of Pediatrics, MIND Institute, University of California, Davis, Sacramento, California, USA.; Shillington A; Cincinnati Children's Hospital Medical Center, Department of Human Genetics, Cincinnati, Ohio, USA.; Cincinnati Children's Hospital Medical Center Department of Psychiatry, Cincinnati, Ohio, USA.; University of Cincinnati College of Medicine Department of Pediatrics, Cincinnati, Ohio, USA.; White L; Cincinnati Children's Hospital Medical Center, Department of Human Genetics, Cincinnati, Ohio, USA.; Elloumi HZ; Clinical Genomics Program, GeneDx, Gaithersburg, Maryland, USA.; Baker PR 2nd; Department of Pediatrics, University of Colorado, Aurora, Colorado, USA.; Svihovec S; Department of Pediatrics, University of Colorado, Aurora, Colorado, USA.; Brown K; Department of Pediatrics, University of Colorado, Aurora, Colorado, USA.; Koopman-Keemink Y; Department of Paediatrics, Juliana Children's Hospital, HAGA Medical Center, the Hague, The Netherlands.; Hoffer MJV; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.; Lakeman IMM; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.; Brischoux-Boucher E; Centre de Genetique Humaine, Universite de Bourgogne Franche-Comte, France.; Kinali M; Department of Brain Sciences, Imperial College London and Portland Hospital HCA International, London, United Kingdom.; Zhao X; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Baylor Genetics, Houston, Texas, USA.; Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas, USA.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Vetro A; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.; Pelorosso C; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.; Balestrini S; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy; University of Florence, Florence, Italy.; Masi A; Department of Neuroscience, Psychology, Drug Research and Child Health (NeuroFarBa), Section of Pharmacology and Toxicology, University of Florence, Florence, Italy.; Hambleton S; Newcastle University Translational and Clinical Research Institute, Newcastle upon Tyne, UK; Great North Children's Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Argilli E; Department of Neurology and Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.; Conti V; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.; Giubbolini S; National Enterprise for NanoScience and NanoTechnology (NEST), Istituto Nanoscienze, Consiglio Nazionale delle Ricerche (CNR) and Scuola Normale Superiore Pisa, Pisa, Italy.; Barrick R; Division of Metabolic Disorders, Children's Hospital of Orange County (CHOC), Orange, CA, USA.; Bergant G; Clinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia.; Writzl K; Clinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia.; Bijlsma EK; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.; Brunet T; Institute of Human Genetics, School of Medicine, Technical University Munich, Munich, Germany; Department of Pediatric Neurology and Developmental Medicine, Dr. v. Hauner Children's Hospital, LMU - University of Munich, München, Germany.; Cacheiro P; William Harvey Research Institute, Queen Mary University of London, London, UK.; Mei D; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy.; Devlin A; Newcastle University Translational and Clinical Research Institute, Newcastle upon Tyne, UK; Great North Children's Hospital, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Hoffer MJV; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.; Machol K; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.; Mannaioni G; Department of Neuroscience, Psychology, Drug Research and Child Health (NeuroFarBa), Section of Pharmacology and Toxicology, University of Florence, Florence, Italy.; Sakamoto M; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama 236-0004 Japan.; Menezes MP; Department of Neurology, The Children's Hospital at Westmead and the Children's Hospital at Westmead Clinical School, University of Sydney, Westmead NSW, Australia.; Courtin T; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, Paris, France; Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, Département de Génétique, DMU BioGeM, Paris, France.; Sherr E; Department of Neurology and Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.; Parra R; National Enterprise for NanoScience and NanoTechnology (NEST), Istituto Nanoscienze, Consiglio Nazionale delle Ricerche (CNR) and Scuola Normale Superiore Pisa, Pisa, Italy.; Richardson R; Northern Genetics Service, Newcastle upon Tyne hospitals NHS Foundation Trust, Newcastle, UK.; Roscioli T; New South Wales Health Pathology Randwick Genomics, Prince of Wales Hospital, Sydney, NSW 2031, Australia; Neuroscience Research Australia, Sydney, NSW 2031, Australia.; Scala M; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; von Stülpnagel C; Department of Pediatric Neurology and Developmental Medicine, Dr. v. Hauner Children's Hospital, LMU - University of Munich, München, Germany; Institute for Transition, Rehabilitation and Palliation, Paracelsus Medical University, Salzburg, Austria.; Smedley D; William Harvey Research Institute, Queen Mary University of London, London, UK.; Torella A; Department of Precision Medicine, University 'Luigi Vanvitelli,' Naples, Italy; Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.; Tohyama J; Department of Child Neurology, Nishi-Niigata Chuo National Hospital, Niigata 950-2085, Japan.; Koichihara R; Department for Child Health and Human Development, Saitama Children's Medical Center, Saitama 330-8777, Japan.; Hamada K; Department of Biochemistry, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.; Ogata K; Department of Biochemistry, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.; Suzuki T; School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Kanagawa, Japan.; Sugie A; Brain Research Institute, Niigata University, Niigata 951-8585, Japan.; van der Smagt JJ; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; van Gassen K; Department of Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.; Valence S; Centre de référence Maladies Rares 'Déficience intellectuelle de cause rare,' Sorbonne Université, Paris, France; Département de Neuropédiatrie, Hôpital Armand Trousseau, APHP, Sorbonne Université, Paris, France.; Vittery E; Northern Genetics Service, Newcastle upon Tyne hospitals NHS Foundation Trust, Newcastle, UK.; Malone S; Department of Neurosciences, Queensland Children's Hospital, Brisbane QLD, Australia; Centre for Advanced Imaging, University of Queensland, St Lucia QLD, Australia.; Kato M; Department of Pediatrics, Showa University School of Medicine, Tokyo 142-8666, Japan.; Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama 236-0004 Japan.; Ratto GM; National Enterprise for NanoScience and NanoTechnology (NEST), Istituto Nanoscienze, Consiglio Nazionale delle Ricerche (CNR) and Scuola Normale Superiore Pisa, Pisa, Italy; Istituto Neuroscienze CNR, Padova, Italy.; Guerrini R; Neuroscience Department, Meyer Children's Hospital IRCCS, Florence, Italy; University of Florence, Florence, Italy. Electronic address: r.guerrini@meyer.it.

Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Rooney K; Verspeeten Clinical Genome Centre, London Health Science Centre, London, ON, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON, Canada.; van der Laan L; Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Trajkova S; Department of Medical Sciences, University of Torino, Torino, Italy.; Haghshenas S; Verspeeten Clinical Genome Centre, London Health Science Centre, London, ON, Canada.; Relator R; Verspeeten Clinical Genome Centre, London Health Science Centre, London, ON, Canada.; Lauffer P; Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Vos N; Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Levy MA; Verspeeten Clinical Genome Centre, London Health Science Centre, London, ON, Canada.; Brunetti-Pierri N; Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy; Department of Translational Medicine, Federico II University, Naples, Italy.; Terrone G; Department of Translational Medicine, Federico II University, Naples, Italy.; Mignot C; Assistance Publique-Hopitaux de Paris, Sorbonne Université, Departement de Génétique, Groupe Hospitalier Pitie-Salpetriere et Hopital Trousseau, Paris, France.; Keren B; Assistance Publique-Hopitaux de Paris, Sorbonne Université, Departement de Génétique, Groupe Hospitalier Pitie-Salpetriere et Hopital Trousseau, Paris, France.; de Villemeur TB; Sorbonne Université, APHP, Hôpital Trousseau, Service de neuropédiatrie, Paris, France.; Volker-Touw CML; Department of Genetics, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.; Verbeek N; Department of Genetics, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.; van der Smagt JJ; Department of Genetics, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.; Oegema R; Department of Genetics, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.; Brusco A; Department of Medical Sciences, University of Torino, Torino, Italy; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, Torino, Italy.; Ferrero GB; Department of Clinical and Biological Science, University of Torino, Torino, Italy.; Misra-Isrie M; Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Hochstenbach R; Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Alders M; Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Mannens MMAM; Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Sadikovic B; Verspeeten Clinical Genome Centre, London Health Science Centre, London, ON, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON, Canada. Electronic address: bekim.sadikovic@lhsc.on.ca.; van Haelst MM; Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Henneman P; Department of Human Genetics, Amsterdam Reproduction and Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands. Electronic address: p.henneman@amsterdamumc.nl.

Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Copier JS; Experimental Cardiology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.; Amsterdam Cardiovascular Sciences, Heart Failure & Arrhythmias, Amsterdam, The Netherlands.; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart: ERN GUARD-Heart'.; Bootsma M; Department of Cardiology, Leiden University Medical Center, Albinusdreef 2, 2300 Leiden, The Netherlands.; Ng CA; Mark Cowley Lidwill Research Program in Cardiac Electrophysiology, Victor Chang Cardiac Research Institute, Darlinghurst, New South Wales, Australia.; School of Clinical Medicine, UNSW Sydney, Darlinghurst, New South Wales, Australia.; Wilde AAM; Experimental Cardiology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.; Amsterdam Cardiovascular Sciences, Heart Failure & Arrhythmias, Amsterdam, The Netherlands.; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart: ERN GUARD-Heart'.; Bertels RA; Department of Paediatric Cardiology, Leiden University Medical Center, Willem-Alexander Children's Hospital, Albinusdreef 2, 2333 Leiden, Netherlands.; Bikker H; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart: ERN GUARD-Heart'.; Human Genetics, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.; Christiaans I; Department of Clinical Genetics, University Medical Centre Groningen, 9713GZ Groningen, The Netherlands.; van der Crabben SN; Human Genetics, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.; Hol JA; Erasmus MC, Clinical Genetics, Doctor Molewaterplein 40, 3015 Rotterdam, The Netherlands.; Koopmann TT; Clinical Genetics, Leiden University Medical Center, Albinusdreef 2, 2333 Leiden, The Netherlands.; Knijnenburg J; Clinical Genetics, Leiden University Medical Center, Albinusdreef 2, 2333 Leiden, The Netherlands.; Lommerse AAJ; Department of Cardiology, Leiden University Medical Center, Albinusdreef 2, 2300 Leiden, The Netherlands.; van der Smagt JJ; Clinical Genetics, University Medical Center Utrecht, Lundlaan 6, Utrecht, The Netherlands.; Bezzina CR; Experimental Cardiology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.; Amsterdam Cardiovascular Sciences, Heart Failure & Arrhythmias, Amsterdam, The Netherlands.; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart: ERN GUARD-Heart'.; Vandenberg JI; Mark Cowley Lidwill Research Program in Cardiac Electrophysiology, Victor Chang Cardiac Research Institute, Darlinghurst, New South Wales, Australia.; School of Clinical Medicine, UNSW Sydney, Darlinghurst, New South Wales, Australia.; Verkerk AO; Experimental Cardiology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.; Amsterdam Cardiovascular Sciences, Heart Failure & Arrhythmias, Amsterdam, The Netherlands.; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart: ERN GUARD-Heart'.; Medical Biology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.; Barge-Schaapveld DQCM; Clinical Genetics, Leiden University Medical Center, Albinusdreef 2, 2333 Leiden, The Netherlands.; Lodder EM; Experimental Cardiology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, Amsterdam, The Netherlands.; Amsterdam Cardiovascular Sciences, Heart Failure & Arrhythmias, Amsterdam, The Netherlands.; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart: ERN GUARD-Heart'.

Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

Hoorntje ET; Department of Genetics, University Medical Centre Groningen, University of Groningen (E.T.H., G.J.t.M., J.D.H.J.).; Netherlands Heart Institute, Utrecht, the Netherlands (E.T.H., L.P.B., L.L., J.P.v.T.).; Burns C; Agnes Ginges Centre for Molecular Cardiology at Centenary Institute (C.B., B.G., R.D.B., C.S.).; Faculty of Medicine and Health (C.B., B.G., R.D.B., J.D., C.S., L.Y., J.I.).; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia (C.B., B.G., C.S., L.Y., J.I.).; Marsili L; Department of Clinical Genetics, Amsterdam University Medical Centre, location AMC, University of Amsterdam, the Netherlands (L.M., J.P.v.T.).; Clinique de Génétique, CHU Lille, Lille, France (L.M.).; Corden B; National Heart and Lung Institute and MRC London Institute of Medical Science, Imperial College London and Cardiovascular Research Centre, Royal Brompton and Harefield NHS Foundation Trust, London, UK (B.C., A.L., N.W., J.S.W.).; Parikh VN; Stanford Centre for Inherited Cardiovascular Disease, Department of Medicine, Stanford University School of Medicine, CA (V.N.P., C.R., E.A.A., M.T.W.).; Te Meerman GJ; Department of Genetics, University Medical Centre Groningen, University of Groningen (E.T.H., G.J.t.M., J.D.H.J.).; Gray B; Agnes Ginges Centre for Molecular Cardiology at Centenary Institute (C.B., B.G., R.D.B., C.S.).; Faculty of Medicine and Health (C.B., B.G., R.D.B., J.D., C.S., L.Y., J.I.).; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia (C.B., B.G., C.S., L.Y., J.I.).; Adiyaman A; Department of Cardiology, Isala Heart Center, Zwolle (A.A.).; Bagnall RD; Agnes Ginges Centre for Molecular Cardiology at Centenary Institute (C.B., B.G., R.D.B., C.S.).; Faculty of Medicine and Health (C.B., B.G., R.D.B., J.D., C.S., L.Y., J.I.).; Barge-Schaapveld DQCM; Department of Clinical Genetics, Leiden University Medical Centre (D.Q.C.M.B.-S., A.M.v.M.).; van den Berg MP; Department of Cardiology, University of Groningen, University Medical Centre Groningen (M.P.v.d.B., G.v.W.).; Bootsma M; Department of Cardiology, University of Leiden, Leiden University Medical Centre (M.B.).; Bosman LP; Netherlands Heart Institute, Utrecht, the Netherlands (E.T.H., L.P.B., L.L., J.P.v.T.).; Department of Cardiology, University of Utrecht (L.P.B.).; Correnti G; Adult Genetics Unit, Royal Adelaide Hospital and Faculty of Health and Medical Sciences, University of Adelaide (G.C.).; Duflou J; Agnes Ginges Centre for Molecular Cardiology at Centenary Institute (C.B., B.G., R.D.B., C.S.).; Eppinga RN; Fatkin D; Victor Chang Cardiac Research Institute, Sydney (D.F.).; Fietz M; Department of Diagnostic Genomics, PathWest Laboratory, Medicine WA, Redlands, Australia (M.F.).; Haan E; Jongbloed JDH; Department of Genetics, University Medical Centre Groningen, University of Groningen (E.T.H., G.J.t.M., J.D.H.J.).; Hauer AD; Department of Cardiology, Haga Teaching Hospital, the Hague (A.D.H.).; Lam L; Netherlands Heart Institute, Utrecht, the Netherlands (E.T.H., L.P.B., L.L., J.P.v.T.).; van Lint FHM; Department of Genetics, University of Utrecht, University Medical Centre Utrecht, the Netherlands (F.H.M.v.L., J.P.v.T.).; Lota A; National Heart and Lung Institute and MRC London Institute of Medical Science, Imperial College London and Cardiovascular Research Centre, Royal Brompton and Harefield NHS Foundation Trust, London, UK (B.C., A.L., N.W., J.S.W.).; Marcelis C; Department of Clinical Genetics, Radboud University Medical Centre, Nijmegen, the Netherlands (C.M.).; McCarthy HJ; Department of Clinical Genetics, Children's Hospital Westmead, Sydney, Australia (H.J.M.).; van Mil AM; Department of Clinical Genetics, Leiden University Medical Centre (D.Q.C.M.B.-S., A.M.v.M.).; Oldenburg RA; Department of Clinical Genetics, Erasmus University Medical Centre, Rotterdam, the Netherlands (R.A.O.).; Pachter N; Genetic Services of Western Australia, Perth, Australia (N.P.).; Planken RN; Department of Radiology and Nuclear Medicine, Amsterdam University Medical Centre, Amsterdam, the Netherlands (R.N.P.).; Reuter C; Stanford Centre for Inherited Cardiovascular Disease, Department of Medicine, Stanford University School of Medicine, CA (V.N.P., C.R., E.A.A., M.T.W.).; Semsarian C; Agnes Ginges Centre for Molecular Cardiology at Centenary Institute (C.B., B.G., R.D.B., C.S.).; Faculty of Medicine and Health (C.B., B.G., R.D.B., J.D., C.S., L.Y., J.I.).; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia (C.B., B.G., C.S., L.Y., J.I.).; van der Smagt JJ; Thompson T; Department of Cardiology and Department of Genomic Medicine, Royal Melbourne Hospital (T.T., J.V., D.Z.).; Vohra J; Department of Cardiology and Department of Genomic Medicine, Royal Melbourne Hospital (T.T., J.V., D.Z.).; Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Australia (J.V., D.Z.).; Volders PGA; Department of Cardiology, Cardiovascular Research Institute Maastricht (CARIM) (P.G.A.V.).; van Waning JI; Whiffin N; National Heart and Lung Institute and MRC London Institute of Medical Science, Imperial College London and Cardiovascular Research Centre, Royal Brompton and Harefield NHS Foundation Trust, London, UK (B.C., A.L., N.W., J.S.W.).; van den Wijngaard A; Department of Clinical Genetics, Laboratory Clinical Genetics, Maastricht University Medical Centre (A.v.d.W.).; Amin AS; Department of Clinical and Experimental Cardiology, Heart Centre, Amsterdam University Medical Centre, location AMC, the Netherlands (A.S.A., A.A.M.W.).; Wilde AAM; Department of Clinical and Experimental Cardiology, Heart Centre, Amsterdam University Medical Centre, location AMC, the Netherlands (A.S.A., A.A.M.W.).; van Woerden G; Department of Cardiology, University of Groningen, University Medical Centre Groningen (M.P.v.d.B., G.v.W.).; Yeates L; Faculty of Medicine and Health (C.B., B.G., R.D.B., J.D., C.S., L.Y., J.I.).; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia (C.B., B.G., C.S., L.Y., J.I.).; Cardio Genomics Program at Centenary Institute, The University of Sydney (L.Y., J.I.).; Zentner D; Department of Cardiology and Department of Genomic Medicine, Royal Melbourne Hospital (T.T., J.V., D.Z.).; Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Australia (J.V., D.Z.).; Ashley EA; Stanford Centre for Inherited Cardiovascular Disease, Department of Medicine, Stanford University School of Medicine, CA (V.N.P., C.R., E.A.A., M.T.W.).; Wheeler MT; Stanford Centre for Inherited Cardiovascular Disease, Department of Medicine, Stanford University School of Medicine, CA (V.N.P., C.R., E.A.A., M.T.W.).; Ware JS; National Heart and Lung Institute and MRC London Institute of Medical Science, Imperial College London and Cardiovascular Research Centre, Royal Brompton and Harefield NHS Foundation Trust, London, UK (B.C., A.L., N.W., J.S.W.).; van Tintelen JP; Netherlands Heart Institute, Utrecht, the Netherlands (E.T.H., L.P.B., L.L., J.P.v.T.).; Department of Clinical Genetics, Amsterdam University Medical Centre, location AMC, University of Amsterdam, the Netherlands (L.M., J.P.v.T.).; Department of Genetics, University of Utrecht, University Medical Centre Utrecht, the Netherlands (F.H.M.v.L., J.P.v.T.).; Ingles J; Faculty of Medicine and Health (C.B., B.G., R.D.B., J.D., C.S., L.Y., J.I.).; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, Australia (C.B., B.G., C.S., L.Y., J.I.).; Cardio Genomics Program at Centenary Institute, The University of Sydney (L.Y., J.I.).; Centre for Population Genomics, Garvan Institute of Medical Research and UNSW Sydney (J.I.).; Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Australia (J.I.).

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

Cox MG; Nelen MR; Wilde AA; Wiesfeld AC; van der Smagt JJ; Loh P; Cramer MJ; Doevendans PA; van Tintelen JP; de Bakker JMT; Hauer RNW

Journal of Cardiovascular Electrophysiology (J CARDIOVASC ELECTROPHYSIOL), Aug2008; 19(8): 775-781. (7p)

Cuinat S; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France. Electronic address: silvestre.cuinat@chu-nantes.fr.; Nizon M; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France.; Isidor B; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France.; Stegmann A; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; van Jaarsveld RH; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; van Gassen KL; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; van der Smagt JJ; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Volker-Touw CML; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Holwerda SJB; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Terhal PA; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Schuhmann S; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.; Vasileiou G; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.; Khalifa M; Genetic Department, Dubai Health Authority, Latifa Women and Children Hospital, Dubai, United Arab Emirates.; Nugud AA; Genetic Department, Dubai Health Authority, Latifa Women and Children Hospital, Dubai, United Arab Emirates.; Yasaei H; Dubai Genetics Center, Pathology and Genetics Department, Dubai Health Authority, Dubai, United Arab Emirates.; Ousager LB; Department of Clinical Genetics & Human Genetics, Odense University Hospital, University of Southern Denmark, Odense, Denmark; Department of Clinical Research, Odense University Hospital, University of Southern Denmark, Odense, Denmark.; Brasch-Andersen C; Department of Clinical Genetics & Human Genetics, Odense University Hospital, University of Southern Denmark, Odense, Denmark; Department of Clinical Research, Odense University Hospital, University of Southern Denmark, Odense, Denmark.; Deb W; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France.; Besnard T; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France.; Simon MEH; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Amsterdam KH; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Verbeek NE; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Matalon D; Department of Pediatric, Division of Medical Genetics, Stanford University and Health Care, Palo Alto, CA.; Dykzeul N; Department of Pediatric, Division of Medical Genetics, Stanford University and Health Care, Palo Alto, CA.; White S; Department of Pediatric, Division of Medical Genetics, Stanford University and Health Care, Palo Alto, CA.; Spiteri E; Department of Pediatric, Division of Medical Genetics, Stanford University and Health Care, Palo Alto, CA.; Devriendt K; Center for Human Genetics, University Hospital Leuven, KU Leuven, O&N I Herestraat 49, Leuven, Belgium.; Boogaerts A; Center for Human Genetics, University Hospital Leuven, KU Leuven, O&N I Herestraat 49, Leuven, Belgium.; Willemsen M; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Brunner HG; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Sinnema M; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; De Vries BBA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Gerkes EH; University Medical Center Groningen, Department of Genetics, University of Groningen, Groningen, The Netherlands.; Pfundt R; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Izumi K; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.; Krantz ID; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.; Xu ZL; Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA.; Murrell JR; Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA.; Valenzuela I; Department of Clinical and Molecular Genetics, Hospital Vall d'Hebron, Barcelona, Spain.; Cusco I; Department of Clinical and Molecular Genetics, Hospital Vall d'Hebron, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, Spain.; Rovira-Moreno E; Department of Clinical and Molecular Genetics, Hospital Vall d'Hebron, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, Spain.; Yang Y; AiLife Diagnostics, Pearland, TX.; Bizaoui V; Clinical Genetics and Neurodevelopmental Disorders, Centre Hospitalier de l'Estran, Pontorson, France.; Patat O; Department of Medical Genetics, Toulouse University Hospital, Toulouse, France.; Faivre L; Centre de référence Anomalies du Développement et Syndromes malformatifs, FHU-TRANSLAD, GAD, CHU Dijon et Université de Bourgogne, Dijon, France; Inserm UMR1231, GAD, Université de Bourgogne, Dijon, France.; Tran-Mau-Them F; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; Inserm UMR1231, GAD, Université de Bourgogne, Dijon, France.; Vitobello A; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; Inserm UMR1231, GAD, Université de Bourgogne, Dijon, France.; Denommé-Pichon AS; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; Inserm UMR1231, GAD, Université de Bourgogne, Dijon, France.; Philippe C; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; Inserm UMR1231, GAD, Université de Bourgogne, Dijon, France.; Bezieau S; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France.; Cogné B; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, Nantes, France; Université de Nantes, Inserm UMR 1087 / CNRS UMR 6291, Institut du thorax, Nantes, France. Electronic address: benjamin.cogne@chu-nantes.fr.

Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Noordermeer T; Center for Benign Haematology, Thrombosis and Haemostasis, Van Creveldkliniek, and.; van Asten I; Center for Benign Haematology, Thrombosis and Haemostasis, Van Creveldkliniek, and.; Central Diagnostic Laboratory, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; Schutgens REG; Center for Benign Haematology, Thrombosis and Haemostasis, Van Creveldkliniek, and.; Lakerveld AJ; Central Diagnostic Laboratory, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; Koekman CA; Central Diagnostic Laboratory, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; Hage KY; Central Diagnostic Laboratory, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; Sebastian SAE; Central Diagnostic Laboratory, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; Huisman A; Central Diagnostic Laboratory, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; van den Heuvel DJ; Department of Molecular Biophysics, Utrecht University, Utrecht, The Netherlands.; Gerritsen HC; Department of Molecular Biophysics, Utrecht University, Utrecht, The Netherlands.; Korporaal SJA; Central Diagnostic Laboratory, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; Bierings M; Department of Stem Cell Transplantation, Utrecht University Children's Hospital, Utrecht University, Utrecht, The Netherlands.; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands; and.; van der Smagt JJ; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; van Gijn ME; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; Urbanus RT; Center for Benign Haematology, Thrombosis and Haemostasis, Van Creveldkliniek, and.

Publisher: American Society of Hematology Country of Publication: United States NLM ID: 101698425 Publication Model: Print Cited Medium: Internet ISSN: 2473-9537 (Electronic) Linking ISSN: 24739529 NLM ISO Abbreviation: Blood Adv Subsets: MEDLINE