학술논문


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'학술논문' 에서 검색결과 1,440건 | 목록 1~20
Reference
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Laurie, StevenSteyaert, Wouterde Boer, ElkePolavarapu, KiranSchuermans, NikaSommer, Anna K.Demidov, GermanEllwanger, KorneliaParamonov, IdaThomas, ColineAretz, StefanBaets, JonathanBenetti, ElisaBullich, GemmaChinnery, Patrick F.Clayton-Smith, JillCohen, EnzoDanis, Danielde Sainte Agathe, Jean-MadeleineDenommé-Pichon, Anne-SophieDiaz-Manera, JordiEfthymiou, StephanieFaivre, LaurenceFernandez-Callejo, MarcosFreeberg, MalloryGarcia-Pelaez, JoséGuillot-Noel, LenaHaack, Tobias B.Hanna, MikeHengel, HolgerHorvath, RitaHoulden, HenryJackson, AdamJohansson, LennartJohari, MridulKamsteeg, Erik-JanKellner, MelanieKleefstra, TjitskeLacombe, DidierLochmüller, HannsLópez-Martín, EstrellaMacaya, AlfonsMarcé-Grau, AnnaMaver, AlešMorsy, HebaMuntoni, FrancescoMusacchia, FrancescoNelson, IsabelleNigro, VincenzoOlimpio, CatarinaOliveira, CarlaPaulasová Schwabová, JaroslavaPauly, Martje G.Peterlin, BorutPeters, SophiaPfundt, RolphPiluso, GiulioPiscia, DavidePosada, ManuelReich, SelinaRenieri, AlessandraRyba, LukasŠablauskas, KarolisSavarese, MarcoSchöls, LudgerSchütz, LeonSteinke-Lange, VerenaStevanin, GiovanniStraub, VolkerSturm, MarcSwertz, Morris A.Tartaglia, Marcote Paske, Iris B. A. W.Thompson, RachelTorella, AnnalauraTrainor, ChristinaUdd, BjarneVan de Vondel, Liedeweivan de Warrenburg, Bartvan Reeuwijk, JeroenVandrovcova, JanaVitobello, AntonioVos, JanetVyhnálková, EmílieWijngaard, RobinWilke, CarloWilliam, DoreenXu, JishuYaldiz, BurcuZalatnai, LucaZurek, BirteBrookes, Anthony J.Evangelista, TeresinhaGilissen, ChristianGraessner, HolmHoogerbrugge, NicolineOssowski, StephanRiess, OlafSchüle, RebeccaSynofzik, MatthisVerloes, AlainMatalonga, LeslieBrunner, Han G.Lohmann, Katjade Voer, Richarda M.Töpf, AnaVissers, Lisenka E.L.M.Beltran, SergiHoischen, Alexander
Nature Medicine. 31(2):478-489
Academic Journal
Laurie, StevenSteyaert, Wouterde Boer, ElkePolavarapu, KiranSchuermans, NikaSommer, Anna K.Demidov, GermanEllwanger, KorneliaParamonov, IdaThomas, ColineAretz, StefanBaets, JonathanBenetti, ElisaBullich, GemmaChinnery, Patrick F.Clayton-Smith, JillCohen, EnzoDanis, Danielde Sainte Agathe, Jean-MadeleineDenommé-Pichon, Anne-SophieDiaz-Manera, JordiEfthymiou, StephanieFaivre, LaurenceFernandez-Callejo, MarcosFreeberg, MalloryGarcia-Pelaez, JoséGuillot-Noel, LenaHaack, Tobias B.Hanna, MikeHengel, HolgerHorvath, RitaHoulden, HenryJackson, AdamJohansson, LennartJohari, MridulKamsteeg, Erik-JanKellner, MelanieKleefstra, TjitskeLacombe, DidierLochmüller, HannsLópez-Martín, EstrellaMacaya, AlfonsMarcé-Grau, AnnaMaver, AlešMorsy, HebaMuntoni, FrancescoMusacchia, FrancescoNelson, IsabelleNigro, VincenzoOlimpio, CatarinaOliveira, CarlaPaulasová Schwabová, JaroslavaPauly, Martje G.Peterlin, BorutPeters, SophiaPfundt, RolphPiluso, GiulioPiscia, DavidePosada, ManuelReich, SelinaRenieri, AlessandraRyba, LukasŠablauskas, KarolisSavarese, MarcoSchöls, LudgerSchütz, LeonSteinke-Lange, VerenaStevanin, GiovanniStraub, VolkerSturm, MarcSwertz, Morris A.Tartaglia, Marcote Paske, Iris B. A. W.Thompson, RachelTorella, AnnalauraTrainor, ChristinaUdd, BjarneVan de Vondel, Liedeweivan de Warrenburg, Bartvan Reeuwijk, JeroenVandrovcova, JanaVitobello, AntonioVos, JanetVyhnálková, EmílieWijngaard, RobinWilke, CarloWilliam, DoreenXu, JishuYaldiz, BurcuZalatnai, LucaZurek, BirteBrookes, Anthony J.Evangelista, TeresinhaGilissen, ChristianGraessner, HolmHoogerbrugge, NicolineOssowski, StephanRiess, OlafSchüle, RebeccaSynofzik, MatthisVerloes, AlainMatalonga, LeslieBrunner, Han G.Lohmann, Katjade Voer, Richarda M.Töpf, AnaVissers, Lisenka E.L.M.Beltran, SergiHoischen, Alexander
Nature Medicine. :1-2
Yépez VA; School of Computation, Information and Technology, Technical University of Munich, Garching, Germany.; Demidov G; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Ellwanger K; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Laurie S; Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.; Universitat de Barcelona, Barcelona, Spain.; Luknárová R; School of Computation, Information and Technology, Technical University of Munich, Garching, Germany.; Joseph Maran MI; Department of Genetics/Epigenetics, Faculty NT, Saarland University, Saarbrücken, Germany.; Hentrich T; Department of Genetics/Epigenetics, Faculty NT, Saarland University, Saarbrücken, Germany.; Sagath L; Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; van der Sanden B; Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Astuti G; Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Neveling K; Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Batlle-Masó L; Infection in Immunocompromised Pediatric Patients Research Group, Vall d'Hebron Research Institute, Barcelona, Spain.; Pediatric Infectious Diseases and Immunodeficiencies Unit, Vall d'Hebron University Hospital, Barcelona, Spain.; Beijer D; Division Translational Genomics of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Tübingen, Germany.; Brechtmann F; School of Computation, Information and Technology, Technical University of Munich, Garching, Germany.; Caballero-Oteyza A; RESIST-Cluster of Excellence 2155 to Hannover Medical School, Satellite Center Freiburg, Freiburg, Germany.; Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center, Faculty of Medicine, Albert Ludwigs University of Freiburg, Freiburg, Germany.; Dabad M; Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.; Universitat de Barcelona, Barcelona, Spain.; Denommé-Pichon AS; Medical Genomics, FHU TRANSLAD, Dijon University Hospital, Dijon, France.; Unit 1231 GAD Team, Inserm, Burgundy Europe University, Dijon, France.; Doornbos C; Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.; Center for Molecular and Biomolecular Informatics, Radboud University Medical Center, Nijmegen, the Netherlands.; Eddafir Z; Applied and Translational Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Applied Translational Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.; Estévez-Arias B; Neuromuscular Disorders Unit, Department of Pediatric Neurology, Hospital Sant Joan de Déu, Barcelona, Spain.; Laboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, Barcelona, Spain.; Kilicarslan OA; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Kolen IHM; Division of Neurodegenerative Diseases and Movement Disorders, Department of Neurology, Faculty of Medicine, Heidelberg University Hospital, Heidelberg, Germany.; Kraß L; School of Computation, Information and Technology, Technical University of Munich, Garching, Germany.; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.; Computational Health Center, Helmholtz Center Munich, Neuherberg, Germany.; Lohmann K; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.; Londhe S; School of Computation, Information and Technology, Technical University of Munich, Garching, Germany.; Computational Health Center, Helmholtz Center Munich, Neuherberg, Germany.; Helmholtz Association, Munich School for Data Science, Munich, Germany.; López-Martín E; Institute of Rare Diseases Research, Spanish Undiagnosed Rare Diseases Cases Program (SpainUDP), Undiagnosed Diseases Network International, Instituto de Salud Carlos III, Madrid, Spain.; Maassen K; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.; Macken W; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.; Martínez-Delgado B; Institute of Rare Diseases Research, Spanish Undiagnosed Rare Diseases Cases Program (SpainUDP), Undiagnosed Diseases Network International, Instituto de Salud Carlos III, Madrid, Spain.; CIBER of Rare Diseases (CIBERER), Madrid, Spain.; Mei D; Department of Neuroscience and Medical Genetics, Meyer Children's Hospital IRCCS, Florence, Italy.; Mertes C; School of Computation, Information and Technology, Technical University of Munich, Garching, Germany.; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.; Minardi R; IRCCS Istituto delle Scienze Neurologiche di Bologna, European Reference Network for Rare and Complex Epilepsies (EpiCARE), Bologna, Italy.; Morsy H; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK.; Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, Egypt.; Mueller JS; Dubowitz Neuromuscular Centre, UCL Great Ormond Street Hospital, London, UK.; Natera-de Benito D; Neuromuscular Disorders Unit, Department of Pediatric Neurology, Hospital Sant Joan de Déu, Barcelona, Spain.; Applied Research in Neuromuscular Diseases, Institut de Recerca Sant Joan de Déu, Barcelona, Spain.; Center for Biomedical Research Network on Rare Diseases (CIBERER), ISCIII, Madrid, Spain.; Nelson I; Centre de Recherche en Myologie, Institut de Myologie, Inserm, Sorbonne Université, Paris, France.; Oud MM; Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Paramonov I; Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.; Universitat de Barcelona, Barcelona, Spain.; Picó D; Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.; Universitat de Barcelona, Barcelona, Spain.; Piscia D; Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.; Universitat de Barcelona, Barcelona, Spain.; Polavarapu K; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Raineri E; Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.; Savarese M; Folkhälsan Research Centre and Medicum, University of Helsinki, Helsinki, Finland.; Smal N; VIB-CMN, Applied and Translational Neurogenomics Group, University of Antwerp, Antwerp, Belgium.; Steehouwer M; Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Steyaert W; Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.; Swertz MA; Department of Genetics, Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.; Thomsen M; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.; Töpf A; John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Van de Vondel L; Peripheral Neuropathy Research Group, University of Antwerp, Antwerp, Belgium.; Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.; Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.; van der Vries G; Department of Genetics, Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.; Vitobello A; Medical Genomics, FHU TRANSLAD, Dijon University Hospital, Dijon, France.; Unit 1231 GAD Team, Inserm, Burgundy Europe University, Dijon, France.; Wilke C; Department of Neurodegeneration, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.; German Center for Neurodegenerative Diseases, Tübingen, Germany.; Zurek B; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; T' Hoen PB; Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.; Center for Molecular and Biomolecular Informatics, Radboud University Medical Center, Nijmegen, the Netherlands.; Matalonga L; Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.; Universitat de Barcelona, Barcelona, Spain.; Vissers LELM; Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.; Gilissen C; Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.; Schulze-Hentrich J; Department of Genetics/Epigenetics, Faculty NT, Saarland University, Saarbrücken, Germany.; Beltran S; Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.; Departament de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.; Esteve-Codina A; Centro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.; Universitat de Barcelona, Barcelona, Spain.; Hoischen A; Department of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Department of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, the Netherlands.; Gagneur J; School of Computation, Information and Technology, Technical University of Munich, Garching, Germany. gagneur@in.tum.de.; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany. gagneur@in.tum.de.; Computational Health Center, Helmholtz Center Munich, Neuherberg, Germany. gagneur@in.tum.de.; Graessner H; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany. holm.graessner@med.uni-tuebingen.de.; Centre for Rare Diseases, University of Tübingen, Tübingen, Germany. holm.graessner@med.uni-tuebingen.de.
Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE; In Process
Academic Journal
Boer, Elke deCohen, EnzoCuesta, IsabelDanis, DanielDenommé-Pichon, Anne-SophieGao, FeiGilissen, ChristianHorvath, RitaJohari, MridulJohanson, LennartLi, ShuangMatalonga, LeslieMorsy, HebaNelson, IsabelleParamonov, IdaPaske, Iris B.A.W. teRobinson, PeterSavarese, MarcoSteyaert, WouterTöpf, AnaTrimouille, Aurélienvan der Velde, Joeri K.Vandrovcova, JanaVitobello, AntonioZurek, BirteAbbot, Kristin M.Banka, SiddharthBenetti, Elisade Boer, ElkeCasari, GiorgioCiolfi, AndreaClayton-Smith, JillDallapiccola, BrunoEllwanger, KorneliaFaivre, LaurenceGraessner, HolmHaack, Tobias B.Hammarsjö, AnnaHavlovicova, MarketaHoischen, AlexanderHugon, AnneJackson, AdamKerstjens, MiekeKleefstra, TjitskeLindstrand, AnnaMartín, Estrella LópezMacek, Milan, Jr.Maystadt, IsabelleMorleo, ManuelaNigro, VicenzoNordgren, AnnPettersson, MariaPinelli, MichelePizzi, SimonePosada, ManuelRadio, Francesca C.Renieri, AlessandraRooryck, CarolineRyba, LukasSanten, Gijs W.E.Schwarz, MartinTartaglia, MarcoThauvin, ChristelTorella, AnnalauraVerloes, AlainVissers, LisenkaVotypka, PavelVyshka, KleaZguro, KristinaYaldiz, BurcuLaurie, Stevede Reuver, RickKwint, MichaelPfundt, RolphWillemsen, Michèl A.A.P.Vries, Bert B.A. deVitobello, A.Vissers, Lisenka E.L.M.
In European Journal of Medical Genetics January 2022 65(1)
Academic Journal
Sommer AK; Institute of Human Genetics, Medical Faculty, University of Bonn, Bonn, Germany.; Te Paske IBAW; Department of Human Genetics, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands; Department of Pathology, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Jansen EAM; Department of Human Genetics, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Gschwind A; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Demidov G; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Steinke-Lange V; MGZ - Medizinisch Genetisches Zentrum, Munich, Germany; Medizinische Klinik und Poliklinik IV - Campus Innenstadt, Klinikum der Universität München, Munich, Germany; European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS), Nijmegen, the Netherlands.; Spier I; Institute of Human Genetics, Medical Faculty, University of Bonn, Bonn, Germany; European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS), Nijmegen, the Netherlands; National Center for Hereditary Tumour Syndromes, University Hospital Bonn, Bonn, Germany.; Steyaert W; Department of Human Genetics, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Yaldiz B; Department of Human Genetics, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Steehouwer M; Department of Human Genetics, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Hommerding O; Institute of Pathology, Medical Faculty, University of Bonn, Bonn, Germany.; Dietrich D; Department of Otolaryngology, Head and Neck Surgery, University Hospital Bonn, University of Bonn, Bonn, Germany.; Peters S; Institute of Human Genetics, Medical Faculty, University of Bonn, Bonn, Germany.; Garcia-Pelaez J; i3S - Instituto de Investigação e Inovação em Saúde da Universidade do Porto, Porto, Portugal; Ipatimup, Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.; Laner A; MGZ - Medizinisch Genetisches Zentrum, Munich, Germany.; Oliveira C; European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS), Nijmegen, the Netherlands; i3S - Instituto de Investigação e Inovação em Saúde da Universidade do Porto, Porto, Portugal; Ipatimup, Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.; Capellá G; Hereditary Cancer Program, Catalan Institute of Oncology, IDIBELL and CIBERONC, Barcelona, Spain.; Nagtegaal ID; Department of Pathology, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; Bläker H; Institute of Pathology, University of Leipzig, Leipzig, Germany.; Ellwanger K; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Hoischen A; Department of Human Genetics, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands; Department of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, the Netherlands.; Gilissen C; Department of Human Genetics, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.; van der Post RS; Department of Pathology, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands; European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS), Nijmegen, the Netherlands.; Kristiansen G; Institute of Pathology, Medical Faculty, University of Bonn, Bonn, Germany.; Hoogerbrugge N; Department of Human Genetics, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands; European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS), Nijmegen, the Netherlands.; Ossowski S; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.; Valle L; European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS), Nijmegen, the Netherlands; Hereditary Cancer Program, Catalan Institute of Oncology, IDIBELL and CIBERONC, Barcelona, Spain.; Holinski-Feder E; MGZ - Medizinisch Genetisches Zentrum, Munich, Germany; Medizinische Klinik und Poliklinik IV - Campus Innenstadt, Klinikum der Universität München, Munich, Germany; European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS), Nijmegen, the Netherlands.; Ligtenberg MJL; Department of Human Genetics, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands; Department of Pathology, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands; European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS), Nijmegen, the Netherlands.; Aretz S; Institute of Human Genetics, Medical Faculty, University of Bonn, Bonn, Germany; European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS), Nijmegen, the Netherlands; National Center for Hereditary Tumour Syndromes, University Hospital Bonn, Bonn, Germany. Electronic address: stefan.aretz@uni-bonn.de.; de Voer RM; Department of Human Genetics, Radboud Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands; European Reference Network on Genetic Tumour Risk Syndromes (ERN GENTURIS), Nijmegen, the Netherlands. Electronic address: Richarda.devoer@radboudumc.nl.
Publisher: W.B. Saunders Country of Publication: United States NLM ID: 0374630 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-0012 (Electronic) Linking ISSN: 00165085 NLM ISO Abbreviation: Gastroenterology Subsets: MEDLINE
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