학술논문
'학술논문'
에서 검색결과 19건 | 목록
1~10
Academic Journal
Vos, T; Barber, RM; Bell, B; Bertozzi-Villa, A; Biryukov, S; Bolliger, I; Charlson, F; Davis, A; Degenhardt, L; Dicker, D; Duan, L; Erskine, H; Feigin, VL; Ferrari, AJ; Fitzmaurice, C; Fleming, T; Graetz, N; Guinovart, C; Haagsma, J; Hansen, GM; Hanson, SW; Heuton, KR; Higashi, H; Kassebaum, N; Kyu, H; Laurie, E; Liang, XF; Lofgren, K; Lozano, R; MacIntyre, MF; Moradi-Lakeh, M; Naghavi, M; Nguyen, G; Odell, S; Ortblad, K; Roberts, DA; Roth, GA; Sandar, L; Serina, PT; Stanaway, JD; Steiner, C; Thomas, B; Vollset, SE; Whiteford, H; Wolock, TM; Ye, PP; Zhou, MG; Avila, MA; Aasvang, GM; Abbafati, C; Ozgoren, AA; Abd-Allah, F; Aziz, MIA; Abera, SF; Aboyans, V; Abraham, JP; Abraham, B; Abubakar, I; Abu-Raddad, LJ; Abu-Rmeileh, NME; Aburto, TC; Achoki, T; Ackerman, IN; Adelekan, A; Ademi, Z; Adou, AK; Adsuar, JC; Arnlov, J; Agardh, EE; Al Khabouri, MJ; Alam, SS; Alasfoor, D; Albittar, MI; Alegretti, MA; Aleman, AV; Alemu, ZA; Alfonso-Cristancho, R; Alhabib, S; Ali, R; Alla, F; Allebeck, P; Allen, PJ; AlMazroa, MA; Alsharif, U; Alvarez, E; Alvis-Guzman, N; Ameli, O; Amini, H; Ammar, W; Anderson, BO; Anderson, HR; Antonio, CAT; Anwari, P; Apfel, H; Arsenijevic, VSA; Artaman, A; Asghar, RJ; Assadi, R; Atkins, LS; Atkinson, C; Badawi, A; Bahit, MC; Bakfalouni, T; Balakrishnan, K; Balalla, S; Banerjee, A; Barker-Collo, SL; Barquera, S; Barregard, L; Barrero, LH; Basu, S; Basu, A; Baxter, A; Beardsley, J; Bedi, N; Beghi, E; Bekele, T; Bell, ML; Benjet, C; Bennett, DA; Bensenor, IM; Benzian, H; Bernabe, E; Beyene, TJ; Bhala, N; Bhalla, A; Bhutta, ZQ; Bienhoff, K; Bikbov, B; Bin Abdulhak, A; Blore, JD; Blyth, FM; Bohensky, MA; Basara, BB; Borges, G; Bornstein, NM; Bose, D; Boufous, S; Bourne, RR; Boyers, LN; Brainin, M; Brauer, M; Brayne, CEG; Brazinova, A; Breitborde, NJK; Brenner, H; Briggs, ADM; Brooks, PM; Brown, J; Brugha, TS; Buchbinder, R; Buckle, GC; Bukhman, G; Bulloch, AG; Burch, M; Burnett, R; Cardenas, R; Cabral, NL; Nonato, IRC; Campuzano, JC; Carapetis, JR; Carpenter, DO; Caso, V; Castaneda-Orjuela, CA; Catala-Lopez, F; Chadha, VK; Chang, JC; Chen, HL; Chen, WQ; Chiang, PP; Chimed-Ochir, O; Chowdhury, R; Christensen, H; Christophi, CA; Chugh, SS; Cirillo, M; Coggeshall, M; Cohen, A; Colistro, V; Colquhoun, SM; Contreras, AG; Cooper, LT; Cooper, C; Cooperrider, K; Coresh, J; Cortinovis, M; Criqui, MH; Crump, JA; Cuevas-Nasu, L; Dandona, R; Dandona, L; Dansereau, E; Dantes, HG; Dargan, PI; Davey, G; Davitoiu, DV; Dayama, A; De la Cruz-Gongora, V; de la Vega, SF; De Leo, D; del Pozo-Cruz, B; Dellavalle, RP; Deribe, K; Derrett, S; Des Jarlais, DC; Dessalegn, M; de Veber, GA; Dharmaratne, SD; Diaz-Torne, C; Ding, EL; Dokova, K; Dorsey, ER; Driscoll, TR; Duber, H; Durrani, AM; Edmond, KM; Ellenbogen, RG; Endres, M; Ermakov, SP; Eshrati, B; Esteghamati, A; Estep, K; Fahimi, S; Farzadfar, F; Fay, DFJ; Felson, DT; Fereshtehnejad, SM; Fernandes, JG; Ferri, CP; Flaxman, A; Foigt, N; Foreman, KJ; Fowkes, FGR; Franklin, RC; Furst, T; Futran, ND; Gabbe, BJ; Gankpe, FG; Garcia-Guerra, FA; Geleijnse, JM; Gessner, BD; Gibney, KB; Gillum, RF; Ginawi, IA; Giroud, M; Giussani, G; Goenka, S; Goginashvili, K; Gona, P; de Cosio, TG; Gosselin, RA; Gotay, CC; Goto, A; Gouda, HN; Guerrant, RL; Gugnani, HC; Gunnell, D; Gupta, R; Gutierrez, RA; Hafezi-Nejad, N; Hagan, H; Halasa, Y; Hamadeh, RR; Hamavid, H; Hammami, M; Hankey, GJ; Hao, YT; Harb, HL; Haro, JM; Havmoeller, R; Hay, RJ; Hay, S; Hedayati, MT; Pi, IBH; Heydarpour, P; Hijar, M; Hoek, HW; Hoffman, HJ; Hornberger, JC; Hosgood, HD; Hossain, M; Hotez, PJ; Hoy, DG; Hsairi, M; Hu, H; Hu, GQ; Huang, JJ; Huang, C; Huiart, L; Husseini, A; Iannarone, M; Iburg, KM; Innos, K; Inoue, M; Jacobsen, KH; Jassal, SK; Jeemon, P; Jensen, PN; Jha, V; Jiang, G; Jiang, Y; Jonas, JB; Joseph, J; Juel, K; Kan, HD; Karch, A; Karimkhani, C; Karthikeyan, G; Katz, R; Kaul, A; Kawakami, N; Kazi, DS; Kemp, AH; Kengne, AP; Khader, YS; Khalifa, SEAH; Khan, EA; Khan, G; Khang, YH; Khonelidze, I; Kieling, C; Kim, D; Kim, S; Kimokoti, RW; Kinfu, Y; Kinge, JM; Kissela, BM; Kivipelto, M; Knibbs, L; Knudsen, AK; Kokubo, Y; Kosen, S; Kramer, A; Kravchenko, M; Krishnamurthi, RV; Krishnaswami, S; Defo, BK; Bicer, BK; Kuipers, EJ; Kulkarni, VS; Kumar, K; Kumar, GA; Kwan, GF; Lai, T; Lalloo, R; Lam, H; Lan, Q; Lansingh, VC; Larson, H; Larsson, A; Lawrynowicz, AEB; Leasher, JL; Lee, JT; Leigh, J; Leung, R; Levi, M; Li, B; Li, YC; Li, YM; Liang, J; Lim, S; Lin, HH; Lind, M; Lindsay, MP; Lipshultz, SE; Liu, SW; Lloyd, BK; Ohno, SL; Logroscino, G; Looker, KJ; Lopez, AD; Lopez-Olmedo, N; Lortet-Tieulent, J; Lotufo, PA; Low, N; Lucas, RM; Lunevicius, R; Lyons, RA; Ma, JX; Ma, S; Mackay, MT; Majdan, M; Malekzadeh, R; Mapoma, CC; Marcenes, W; March, LM; Margono, C; Marks, GB; Marzan, MB; Masci, JR; Mason-Jones, AJ; Matzopoulos, RG; Mayosi, BM; Mazorodze, TT; McGill, NW; McGrath, JJ; McKee, M; McLain, A; McMahon, BJ; Meaney, PA; Mehndiratta, MM; Mejia-Rodriguez, F; Mekonnen, W; Melaku, YA; Meltzer, M; Memish, ZA; Mensah, G; Meretoja, A; Mhimbira, FA; Micha, R; Miller, TR; Mills, EJ; Mitchell, PB; Mock, CN; Moffitt, TE; Ibrahim, NM; Mohammad, KA; Mokdad, AH; Mola, GL; Monasta, L; Montico, M; Montine, TJ; Moore, AR; Moran, AE; Morawska, L; Mori, R; Moschandreas, J; Moturi, WN; Moyer, M; Mozaffarian, D; Mueller, UO; Mukaigawara, M; Murdoch, ME; Murray, J; Murthy, KS; Naghavi, P; Nahas, Z; Naheed, A; Naidoo, KS; Naldi, L; Nand, D; Nangia, V; Narayan, KMV; Nash, D; Nejjari, C; Neupane, SP; Newman, LM; Newton, CR; Ng, M; Ngalesoni, FN; Nhung, NT; Nisar, MI; Nolte, S; Norheim, OF; Norman, RE; Norrving, B; Nyakarahuka, L; Oh, IH; Ohkubo, T; Omer, SB; Opio, JN; Ortiz, A; Pandian, JD; Panelo, CIA; Papachristou, C; Park, EK; Parry, CD; Caicedo, AJP; Patten, SB; Paul, VK; Pavlin, BI; Pearce, N; Pedraza, LS; Pellegrini, CA; Pereira, DM; Perez-Ruiz, FP; Perico, N; Pervaiz, A; Pesudovs, K; Peterson, CB; Petzold, M; Phillips, MR; Phillips, D; Phillips, B; Piel, FB; Plass, D; Poenaru, D; Polanczyk, GV; Polinder, S; Pope, CA; Popova, S; Poulton, RG; Pourmalek, F; Prabhakaran, D; Prasad, NM; Qato, D; Quistberg, DA; Rafay, A; Rahimi, K; Rahimi-Movaghar, V; Rahman, SU; Raju, M; Rakovac, I; Rana, SM; Razavi, H; Refaat, A; Rehm, J; Remuzzi, G; Resnikoff, S; Ribeiro, AL; Riccio, PM; Richardson, L; Richardus, JH; Riederer, AM; Robinson, M; Roca, A; Rodriguez, A; Rojas-Rueda, D; Ronfani, L; Rothenbacher, D; Roy, N; Ruhago, GM; Sabin, N; Sacco, RL; Ksoreide, K; Saha, S; Sahathevan, R; Sahraian, MA; Sampson, U; Sanabria, JR; Sanchez-Riera, L; Santos, IS; Satpathy, M; Saunders, JE; Sawhney, M; Saylan, MI; Scarborough, P; Schoettker, B; Schneider, IJ; Schwebel, DC; Scott, JG; Seedat, S; Sepanlou, SG; Serdar, B; Servan-Mori, EE; Shackelford, K; Shaheen, A; Shahraz, S; Levy, TS; Shangguan, S; She, J; Sheikhbahaei, S; Shepard, DS; Shi, PL; Shibuya, K; Shinohara, Y; Shiri, R; Shishani, K; Shiue, I; Shrime, MG; Sigfusdottir, ID; Silberberg, DH; Simard, EP; Sindi, S; Singh, JA; Singh, L; Skirbekk, V; Sliwa, K; Soljak, M; Soneji, S; Soshnikov, SS; Speyer, P; Sposato, LA; Sreeramareddy, CT; Stoeckl, H; Stathopoulou, VK; Steckling, N; Stein, MB; Stein, DJ; Steiner, TJ; Stewart, A; Stork, E; Stovner, LJ; Stroumpoulis, K; Sturua, L; Sunguya, BF; Swaroop, M; Sykes, BL; Tabb, KM; Takahashi, K; Tan, F; Tandon, N; Tanne, D; Tanner, M; Tavakkoli, M; Taylor, HR; Ao, BJT; Temesgen, AM; Ten Have, M; Tenkorang, EY; Terkawi, AS; Theadom, AM; Thomas, E; Thorne-Lyman, AL; Thrift, AG; Tleyjeh, IM; Tonelli, M; Topouzis, F; Towbin, JA; Toyoshima, H; Traebert, J; Tran, BX; Trasande, L; Trillini, M; Truelsen, T; Trujillo, U; Tsilimbaris, M; Tuzcu, EM; Ukwaja, KN; Undurraga, EA; Uzun, SB; van Brakel, WH; de Vijver, SV; Van Dingenen, R; van Gool, CH; Varakin, YY; Vasankari, TJ; Vavilala, MS; Veerman, LJ; Velasquez-Melendez, G; Venketasubramanian, N; Vijayakumar, L; Villalpando, S; Violante, FS; Vlassov, VV; Waller, S; Wallin, MT; Wan, X; Wang, LH; Wang, JL; Wang, YP; Warouw, TS; Weichenthal, S; Weiderpass, E; Weintraub, RG; Werdecker, A; Wessells, KRR; Westerman, R; Wilkinson, JD; Williams, HC; Williams, TN; Woldeyohannes, SM; Wolfe, CDA; Wong, JQ; Wong, HD; Woolf, AD; Wright, JL; Wurtz, B; Xu, GL; Yang, GH; Yano, Y; Yenesew, MA; Yentur, GK; Yip, P; Yonemoto, N; Yoon, SJ; Younis, M; Yu, CH; Kim, KY; Zaki, MES; Zhang, Y; Zhao, Z; Zhao, Y; Zhu, J; Zonies, D; Zunt, JR; Salomon, JA; Murray, CJL
Lancet (London, England). 386(9995):743-800
Academic Journal
Rafay MF; Cortez MA; de Veber GA; Tan-Dy C; Al-Futaisi A; Yoon W; Fallah S; Moore AM; Rafay, Mubeen F; Cortez, Miguel A; de Veber, Gabrielle A; Tan-Dy, Cherrie; Al-Futaisi, Amna; Yoon, Woojin; Fallah, Shafagh; Moore, Aideen M
Academic Journal
Academic Journal
Lecoquierre F; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France. francois.lecoquierre@chu-rouen.fr.; Centre de Ressources Biologiques institutionnel du CHU de Rouen - Biothèque filière génétique, Rouen, France. francois.lecoquierre@chu-rouen.fr.; Cassinari K; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Drouot N; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; May A; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Fourneaux S; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Charbonnier F; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Derambure C; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Coutant S; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Saugier-Veber P; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Hoischen A; Department of Human Genetics, Radboud University Medical Center, 6525 GA, Nijmegen, The Netherlands.; Charbonnier C; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.; Nicolas G; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and reference center for developmental disorders, F-76000, Rouen, France.
Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
Academic Journal
Aref-Eshghi E; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.; Kerkhof J; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.; Pedro VP; Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON N6A5C1, Canada.; Barat-Houari M; Autoinflammatory and Rare Diseases Unit, Medical Genetic Department for Rare Diseases and Personalized Medicine, Centre Hospitalier Universitaire de Montpellier, 34090 Montpellier, France.; Ruiz-Pallares N; Autoinflammatory and Rare Diseases Unit, Medical Genetic Department for Rare Diseases and Personalized Medicine, Centre Hospitalier Universitaire de Montpellier, 34090 Montpellier, France.; Andrau JC; Institut de Génétique Moléculaire de Montpellier (IGMM), University Montpellier, CNRS-UMR5535, 34090 Montpellier, France.; Lacombe D; Medical Genetics Department, Inserm U1211, Reference Center AD SOOR, AnDDI-RARE, Bordeaux University, Centre Hospitalier Universitaire de Bordeaux, 33076 Bordeaux, France.; Van-Gils J; Medical Genetics Department, Inserm U1211, Reference Center AD SOOR, AnDDI-RARE, Bordeaux University, Centre Hospitalier Universitaire de Bordeaux, 33076 Bordeaux, France.; Fergelot P; Medical Genetics Department, Inserm U1211, Reference Center AD SOOR, AnDDI-RARE, Bordeaux University, Centre Hospitalier Universitaire de Bordeaux, 33076 Bordeaux, France.; Dubourg C; Service de Génétique Moléculaire et Génomique, Centre Hospitalier Universitaire de Rennes, 35000 Rennes, France.; Cormier-Daire V; Department of Medical Genetics, Paris Descartes University, INSERM UMR 1163, Imagine Institute, Necker Enfants Malades Hospital, 75015 Paris, France.; Rondeau S; Department of Medical Genetics, Paris Descartes University, INSERM UMR 1163, Imagine Institute, Necker Enfants Malades Hospital, 75015 Paris, France.; Lecoquierre F; Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, F 76000, Normandy Center for Genomic and Personalized Medicine, 76183 Rouen, France.; Saugier-Veber P; Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, F 76000, Normandy Center for Genomic and Personalized Medicine, 76183 Rouen, France.; Nicolas G; Normandie University, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics and Reference Center for Developmental Disorders, F 76000, Normandy Center for Genomic and Personalized Medicine, 76183 Rouen, France.; Lesca G; Department of Medical Genetics, University Hospital of Lyon, 69007 Lyon, France.; Chatron N; Department of Medical Genetics, University Hospital of Lyon, 69007 Lyon, France.; Sanlaville D; Department of Medical Genetics, University Hospital of Lyon, 69007 Lyon, France.; Vitobello A; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, 15 boulevard du Maréchal de Lattre de Tassigny, 21000, Dijon Cedex, France; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, Dijon University Hospital, 21000 Dijon, France.; Faivre L; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, 15 boulevard du Maréchal de Lattre de Tassigny, 21000, Dijon Cedex, France; Centre de Référence Déficiences Intellectuelles de Causes Rares, CHU Dijon, 21000, Dijon, France.; Thauvin-Robinet C; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, 15 boulevard du Maréchal de Lattre de Tassigny, 21000, Dijon Cedex, France; Centre de Référence Déficiences Intellectuelles de Causes Rares, CHU Dijon, 21000, Dijon, France.; Laumonnier F; UMR 1253, iBrain, Universite de Tours, Inserm, 37200 Tours, France; Centre Hospitalier Universitaire de Tours, Service de Genetique, 37000 Tours, France.; Raynaud M; UMR 1253, iBrain, Universite de Tours, Inserm, 37200 Tours, France; Centre Hospitalier Universitaire de Tours, Service de Genetique, 37000 Tours, France.; Alders M; Amsterdam University Medical Center, University of Amsterdam, Department of Clinical Genetics, Amsterdam Reproduction and Development Research Institute, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.; Mannens M; Amsterdam University Medical Center, University of Amsterdam, Department of Clinical Genetics, Amsterdam Reproduction and Development Research Institute, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.; Henneman P; Amsterdam University Medical Center, University of Amsterdam, Department of Clinical Genetics, Amsterdam Reproduction and Development Research Institute, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.; Hennekam RC; Department of Pediatrics, Academic Medical Center, University of Amsterdam, Amsterdam, 1012 WX, the Netherlands.; Velasco G; Université de Paris, Epigénétique et Destin Cellulaire, CNRS, 75013 Paris, France.; Francastel C; Université de Paris, Epigénétique et Destin Cellulaire, CNRS, 75013 Paris, France.; Ulveling D; Université de Paris, Epigénétique et Destin Cellulaire, CNRS, 75013 Paris, France.; Ciolfi A; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00146 Rome, Italy.; Pizzi S; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00146 Rome, Italy.; Tartaglia M; Genetics and Rare Diseases Research Division, Ospedale Pediatrico Bambino Gesù, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00146 Rome, Italy.; Heide S; Department of Genetics, Referral Center for Intellectual Disabilities, APHP Sorbonne University, Pitié Salpêtrière Hospital, 75013 Paris, France.; Héron D; Department of Genetics, Referral Center for Intellectual Disabilities, APHP Sorbonne University, Pitié Salpêtrière Hospital, 75013 Paris, France.; Mignot C; Department of Genetics, Referral Center for Intellectual Disabilities, APHP Sorbonne University, Pitié Salpêtrière Hospital, 75013 Paris, France.; Keren B; Department of Genetics, Referral Center for Intellectual Disabilities, APHP Sorbonne University, Pitié Salpêtrière Hospital, 75013 Paris, France.; Whalen S; Unit of Genetics, APHP Sorbonne University, Trousseau Hospital, 75012 Paris, France.; Afenjar A; Unit of Genetics, APHP Sorbonne University, Trousseau Hospital, 75012 Paris, France.; Bienvenu T; Department of Molecular Genetics, Cochin Hospital, 75014 Paris, France.; Campeau PM; Department of Pediatrics, University of Montreal, Montreal, QC H3T1J4, Canada.; Rousseau J; Department of Pediatrics, University of Montreal, Montreal, QC H3T1J4, Canada.; Levy MA; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada.; Brick L; Genetic Division, Department of Pediatrics, McMaster University, Hamilton, ON L8S4K1, Canada.; Kozenko M; Genetic Division, Department of Pediatrics, McMaster University, Hamilton, ON L8S4K1, Canada.; Balci TB; Department of Pediatrics, Division of Medical Genetics, Western University, London, ON N6A 3K7; Medical Genetics Program of Southwestern Ontario, London Health Sciences Centre, London, ON N6A5W9, Canada.; Siu VM; Department of Pediatrics, Division of Medical Genetics, Western University, London, ON N6A 3K7; Medical Genetics Program of Southwestern Ontario, London Health Sciences Centre, London, ON N6A5W9, Canada.; Stuart A; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada.; Kadour M; Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A5W9 Canada; St. Joseph's Health Care London, London, ON N6A5W9 Canada.; Masters J; Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A5W9 Canada; St. Joseph's Health Care London, London, ON N6A5W9 Canada.; Takano K; Center for Medical Genetics, Shinshu University Hospital, 3-1-1 Asahi, Matsumoto, Nagano 3908621, Japan.; Kleefstra T; Department of Human Genetics, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands; Donders Center for Medical Neuroscience, 6525 GA Nijmegen, the Netherlands.; de Leeuw N; Department of Human Genetics, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands; Donders Center for Medical Neuroscience, 6525 GA Nijmegen, the Netherlands.; Field M; Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW 2298, Australia.; Shaw M; School of Medicine, Robinson Research Institute, University of Adelaide, Adelaide, SA 5005, Australia.; Gecz J; School of Medicine, Robinson Research Institute, University of Adelaide, Adelaide, SA 5005, Australia; South Australian Health and Medical Research Institute, Adelaide, SA 5005, Australia.; Ainsworth PJ; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada.; Lin H; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada.; Rodenhiser DI; Children's Health Research Institute, London, ON N6A3K7, Canada; Department of Biochemistry, Western University, London, ON N6A3K7, Canada.; Friez MJ; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Tedder M; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Lee JA; Greenwood Genetic Center, Greenwood, SC 29646, USA.; DuPont BR; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Stevenson RE; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Skinner SA; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Schwartz CE; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Genevieve D; Medical Genetic Department for Rare Diseases and Personalized Medicine, Reference Center AD SOOR, AnDDI-RARE, Groupe DI, Inserm U1183-Institute for Regenerative Medicine and Biotherapy, Montpellier University, Centre Hospitalier Universitaire de Montpellier, 34090 Montpellier, France.; Sadikovic B; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, London, ON N6A5W9, Canada; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A3K7, Canada. Electronic address: Bekim.Sadikovic@lhsc.on.ca.
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
Academic Journal
Publisher: Dustri-Verlag Dr. Karl Feistle Country of Publication: Germany NLM ID: 0364441 Publication Model: Print Cited Medium: Print ISSN: 0301-0430 (Print) Linking ISSN: 03010430 NLM ISO Abbreviation: Clin Nephrol Subsets: MEDLINE
Academic Journal
Publisher: Pitman Publishing Country of Publication: England NLM ID: 0355210 Publication Model: Print Cited Medium: Print ISSN: 0071-2736 (Print) Linking ISSN: 00712736 NLM ISO Abbreviation: Proc Eur Dial Transplant Assoc Subsets: MEDLINE
Academic Journal
Publisher: American Medical Association Country of Publication: United States NLM ID: 7501160 Publication Model: Print Cited Medium: Print ISSN: 0098-7484 (Print) Linking ISSN: 00987484 NLM ISO Abbreviation: JAMA Subsets: MEDLINE
Academic Journal
Publisher: Massachusetts Medical Society Country of Publication: United States NLM ID: 0255562 Publication Model: Print Cited Medium: Print ISSN: 0028-4793 (Print) Linking ISSN: 00284793 NLM ISO Abbreviation: N Engl J Med Subsets: MEDLINE
Academic Journal
Cardella CJ; de Veber GA; Hollenberg C; Marshall WJ; Seaver R; Robinette MA; Lindberg MC; Stiller CR
Publisher: Elsevier Science Inc Country of Publication: United States NLM ID: 0243532 Publication Model: Print Cited Medium: Print ISSN: 0041-1345 (Print) Linking ISSN: 00411345 NLM ISO Abbreviation: Transplant Proc Subsets: MEDLINE
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자료유형(Source Type)
주제어
언어