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In: Journal of Research Development in Nursing and Midwifery. (Journal of Research Development in Nursing and Midwifery, May 2021, 18(1):53-57)
Academic Journal
Acharya A; Center for Statistical Genetics, Gertrude H. Sergievsky Center and the Department of Neurology, Columbia University Medical Center, New York, New York, USA.; Kavus H; Department of Pediatrics, Columbia University, New York, New York, USA.; Dunn P; The George Washington University, Washington, District of Columbia, USA.; Nasir A; Department of Molecular Science and Technology, Ajou University, Suwon, The Republic of Korea.; Folk L; GeneDx, Gaithersburg, Maryland, USA.; Withrow K; GeneDx, Gaithersburg, Maryland, USA.; Wentzensen IM; GeneDx, Gaithersburg, Maryland, USA.; Ruzhnikov MRZ; Neurology and Neurological Sciences, Pediatrics, Division of Medical Genetics, Stanford University and Lucile Packard Children's Hospital, Palo Alto, California, USA.; Fallot C; Clinique de Neuropédiatrie, CHU Lille, Lille, France.; Smol T; Institut de Génétique, Univ Lille, EA7364 RADEME, CHU Lille, Lille, France.; Rama M; Institut de Génétique, CHU Lille, Lille, France.; Brown K; Pediatrics-Clinical Genetics and Metabolism, School of Medicine, University of Colorado-Anschutz Medical Campus, Aurora, Colorado, USA.; Whalen S; UF de génétique Clinique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Assistance Publique-Hôpitaux de Paris (APHP) Sorbonne Université, Hôpital Armand Trousseau, ERN-ITHACA, Paris, France.; Ziegler A; Department of Genetics, Angers University Hospital, Angers, France.; Barth M; Department of Genetics, Angers University Hospital, Angers, France.; Chassevent A; Division of Neurogenetics, Kennedy Krieger Institute, Baltimore, Maryland, USA.; Smith-Hicks C; Division of Neurogenetics, Kennedy Krieger Institute, Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Afenjar A; Assistance Publique-Hôpitaux de Paris (APHP) Sorbonne Université, Centre de Référence Malformations et maladies congénitales du cervelet et déficiences intellectuelles de causes rares, département de génétique et embryologie médicale, Hôpital Trousseau, Paris, France.; Courtin T; Département de génétique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (APHP), Paris, France.; Heide S; Department of Genetics, Pitié-Salpêtrière Hospital, Referral Center for Intellectual Disabilities of Rare Causes, Assistance Publique-Hôpitaux de Paris (APHP) Sorbonne Université, Paris, France.; Font-Montgomery E; University Hospital Medical Genetics Clinic, University of Missouri, Columbia, Missouri, USA.; Heid C; University Hospital Medical Genetics Clinic, University of Missouri, Columbia, Missouri, USA.; Hamm JA; Pediatric Genetics, East Tennessee Children's Hospital, Knoxville, Tennessee, USA.; Love DR; Pathology Genetics, Sidra Medicine, Doha, Qatar.; Thabet F; Pediatric Neurology Division, Sidra Medicine, Doha, Qatar.; Misra VK; Department of Pediatrics, Division of Genetic, Genomic, and Metabolic Disorders, Children's Hospital of Michigan, Detroit, Michigan, USA.; Discipline of Pediatrics, Central Michigan University, Mount Pleasant, Michigan, USA.; Cunningham M; Department of Pediatrics, Division of Genetic, Genomic, and Metabolic Disorders, Children's Hospital of Michigan, Detroit, Michigan, USA.; Leal SM; Center for Statistical Genetics, Gertrude H. Sergievsky Center and the Department of Neurology, Columbia University Medical Center, New York, New York, USA.; Taub Institute for Alzheimer's Disease and the Aging Brain, Columbia University Medical Center, New York, New York, USA.; Jarvela I; Department of Medical Genetics, University of Helsinki, Helsinki, Finland.; Normand EA; GeneDx, Gaithersburg, Maryland, USA.; Zou F; GeneDx, Gaithersburg, Maryland, USA.; Helal M; Department of Pediatrics, Columbia University, New York, New York, USA.; Keren B; Département de génétique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (APHP), Paris, France.; Torti E; GeneDx, Gaithersburg, Maryland, USA.; Chung WK; Department of Pediatrics, Columbia University, New York, New York, USA is2632@cumc.columbia.edu wkc15@cumc.columbia.edu.; Department of Medicine, Columbia University, New York, New York, USA.; Schrauwen I; Center for Statistical Genetics, Gertrude H. Sergievsky Center and the Department of Neurology, Columbia University Medical Center, New York, New York, USA is2632@cumc.columbia.edu wkc15@cumc.columbia.edu.
Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE
Abbasi, SorayaAfshar, YaldaAhn, Sun-YoungAlbertine, Kurt H.Allegaert, KarelAlper, Seth L.Altit, GabrielAlvaro, Ruben E.Alvira, Cristina M.Maia Amorim, Natália CarlosAnbuhl, Kelsey L.Andersen, Claus YdingAnderson, Richard A.Andrews, Katrina A.Askenazi, David J.Fernandes Assunção, Débora GabrielaAuten, Richard Lambert, Jr.Autmizguine, JulieAzhibekov, TimurBack, Stephen A.Bahr, Timothy M.Baker, Peter Russell, IIBancalari, Eduardo H.Barichello, TatianaBattaglia, Frederick C.Bauer, Andrew J.Baum, MichelBavis, Ryan W.Beardsall, KathrynBeggs, SimonBenchimol, CorinneBenders, Manon J.N.L.Bennet, LauraBennett, Phillip R.Berger, MelvinBernhard, WolfgangBertram, John F.Bhombal, ShaziaBhutani, Vinod K.Black, Mary JaneBliss, Joseph M.Bolender, David L.Bowdin, Sarah C.Boyd, Scott D.Brandenburg, Joline E.Brown, Laura D.Burrin, Douglas G.Cannon, BarbaraCaplan, MichaelCarlson, Susan E.Carlton, David P.Chaemsaithong, PiyaChang, JillCharlton, Jennifer R.Chemtob, SylvainChheda, SadhanaChilds, Andrew J.Chu, David H.Chung, Wendy K.Cilio, Maria RobertaClark, David A.Clarke, PaulCleal, Jane K.Clemente, Ethel G.Clements, John A.Clyman, Ronald I.Cohen, Jennifer L.Cohen, Susan S.Collins, AmélieCollodel, AllanColombo, JohnCombes, Alexander N.Copp, Andrew J.Cotten, C. MichaelCrawford, Peter A.Crowe, James E., Jr.Crowther, C.A.Cullen-McEwen, Luise A.Cutfield, Wayne S.Cyr-Depauw, ChanèleDanielly da S. Ribeiro, KarlaDauby, NicolasDavenport, PatriciaDavidson, Joanne O.Cruz, Diomel de laGomes de Oliveira, Priscilade Vrijer, BarbraDel Colle, AndrewDelacourt, ChristopheDiacovo, Thomas G.Disdier, ClémenceDormans, John P.Duhamel, FrançoisDuong, Minh DienDysart, KevinEichenwald, Eric C.El-Khuffash, Afif F.Ivor Ellis, Peter JamesEmpey, Kerry M.Ercal, BarisErdős, MelindaErrede, MariellaFeldman, Brian J.Fidanza, MarioFogarty, Matthew J.Friedlich, Philippe S.Fujiwara, RyoichiGallo, VittorioGanguly, AbhrajitGao, YuanshengGarland, MarianneGeddes, DonnaDip (Sci), Post GradGeorgieff, Michael K.Gien, JasonGiussani, Dino A.Goldman, Armond S.Gomez-Lopez, NardhyGood, MistyGood, Pamela I.Gordon, Scott M.Green, Lucy R.Greene, Nicholas D.E.Gridneva, ZoyaGrigoriou, EmmanouilGrimberg, AddaGrunau, Ruth E.Guignard, Jean-PierreGunn, Alistair J.Gurtunca, NursenGustafson, Kathleen M.Hadchouel, AliceHaddad, Gabriel G.Hale, Thomas W.Hambidge, K. MichaelHammerman, CathyRuud Hansen, Thor WillyHanson, Mark A.Harbeson, DannyHarding, J.E.Harding, RichardHarris, Mary CatherineHartmann, PeterHartnett, M. ElizabethHasbun, RodrigoHaugen, GuttormHawkes, Colin P.Hay, William W., Jr.Heine, Vivi M.Helmrath, Michael A.Hendricks-Muñoz, Karen D.Herrera, EmilioHiatt, Michael J.Hooper, Stuart B.Hooven, Thomas A.Iacobelli, SilviaInder, Terrie E.Iruela-Arispe, M. LuisaJadcherla, Sudarshan RaoJain, DeepakJetton, Jennifer G.Jobe, Alan H.Jones, HelenJose, Pedro A.Jung, EunjungKallapur, Suhas G.Kaplan, MichaelKarumanchi, S. AnanthKaskel, Frederick J.Levitt Katz, Lorraine E.Kavus, HalukKeeney, Susan E.Kern, Steven E.Khanjani, ShirinKhlevner, JulieKilpatrick, Laurie E.Kim, Chang-RyulKingma, Paul S.Kinsella, John P.Kiserud, TorvidKoenig, Joyce M.Kohli, RohitKollmann, Tobias R.Kolls, Jay K.Konecny, Christina M.Kratimenos, PanagiotisKrebs, Nancy F.Krutsch, KaytlinKuhn-Riordon, KaraKulik, Thomas J.Kumar, T. RajendraKutikov, Jessica KatzLakshminrusimha, SatyanLasunción, Miguel AngelLavoie, Pascal M.Lawrence, Shelley M.Lee, Mark K.Lee, Mary M.Lee, Yvonne K.Leibel, Sandra L.Levy, OferLevy, Philip T.Lewis, Rohan M.Li, ChanggongLin, FangmingLobritto, StevenLoomis, Cynthia A.MacFarlane, Peter M.MacIntyre, David A.Mahe, Maxime M.Mamsen, Linn SaltoMankouski, AnastasiyaMantilla, Carlos B.Marchant, ArnaudMargolis, Kara GrossMaródi, LászlóMaršál, KarelMartin, Richard J.Martin Carli, Jayne F.Martinez, Hugo R.Matsell, Douglas G.Matthews, Dwight E.McArdle, Harry J.McKinlay, C.J.D.McManaman, James L.McNamara, Patrick J.Meschia, GiacomoMestan, KarenMiller, Steven P.Minoo, ParvizMir, Imran N.Mitchell, Lisa J.Mižíková, IvanaMizuno, TomoyukiMomper, Jeremiah D.Monagle, PaulMonks, JeniferMortola, Jacopo P.Muglia, Louis J.Munshi, Upender K.Narasimhan, SumanaNarendran, VivekNedergaard, JanNelin, Leif D.Neu, JosefNielsen, Sandra C.A.Nigam, Sanjay K.Nizet, VictorNogee, Lawrence M.Noori, ShahabNorris, Andrew W.O’Brien, Barbara M.O’Brien, Lori L.O’Callaghan, Karen M.Ogilvy-Stuart, AmandaOhls, Robin K.Ortega-Senovilla, HenarO’Sullivan, Justin M.Panitch, Howard B.Penn, Anna A.Penn, Raymond B.Petroff, Margaret G.Philipps, Anthony F.Pisani, FrancescoPleasure, DavidPomeroy, Scott L.Post, MartinPrakash, Y.S.Prozialeck, Joshua D.Pysher, Theodore J.Quigley, RaymondRabinovitch, MarleneRaffay, Thomas M.Raj, J. 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In Fetal and Neonatal Physiology Edition: Sixth Edition. 2022:vi-xxx
Academic Journal
Okur V; Division of Molecular Genetics, Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.; Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, TX, USA.; Hamm L; Division of Molecular Genetics, Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.; Kavus H; Division of Molecular Genetics, Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.; Mebane C; Division of Molecular Genetics, Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.; Robinson S; Division of Molecular Genetics, Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.; Levy B; Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.; Chung WK; Division of Molecular Genetics, Department of Pediatrics, Columbia University Medical Center, New York, NY, USA. wkc15@cumc.columbia.edu.; Department of Medicine, Columbia University Medical Center, New York, NY, USA. wkc15@cumc.columbia.edu.
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
Academic Journal
Garrity M; Columbia University School of Dental Medicine, New York, New York 10032, USA.; Kavus H; Department of Pediatrics, Columbia University Medical Center, New York, New York 10032, USA.; Rojas-Vasquez M; Department of Pediatric Hematology-Oncology, Stollery Children's Hospital, Edmonton, Alberta T6G 2B7, Canada.; Valenzuela I; Department of Clinical and Molecular Genetics, Hospital Vall d'Hebron, 08035 Barcelona, Spain.; Larson A; Section of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado, Aurora, Colorado 80045, USA.; Reed S; Clinical Genetics and Genomic Medicine, Geisinger Health System, Danville, Pennsylvania 17821, USA.; Bellus G; Clinical Genetics and Genomic Medicine, Geisinger Health System, Danville, Pennsylvania 17821, USA.; Mignot C; APHP-Sorbonne Université, Département de Génétique, Hôpital Trousseau et Groupe Hospitalier Pitié-Salpêtrière, 75013 Paris, France.; Munnich A; Imagine Institute, INSERM UMR 1163, Université de Paris; Fédération de Génétique Médicale, Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, 75015 Paris, France.; Isidor B; Service de Génétique Médicale, CHU Nantes, 44093 Nantes Cedex 1, France.; L'Institut du Thorax, INSERM, CNRS, Université de Nantes, 44007 Nantes, France.; Chung WK; Department of Pediatrics, Columbia University Medical Center, New York, New York 10032, USA.; Department of Medicine, Columbia University Medical Center, New York, New York 10032, USA.
Publisher: Cold Spring Harbor Laboratory Press Country of Publication: United States NLM ID: 101660017 Publication Model: Electronic-Print Cited Medium: Internet ISSN: 2373-2873 (Electronic) Linking ISSN: 23732873 NLM ISO Abbreviation: Cold Spring Harb Mol Case Stud Subsets: MEDLINE
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