학술논문

발행년
-
(예 : 2010-2015)
'학술논문' 에서 검색결과 19건 | 목록 1~10
Academic Journal
Vos, TBarber, RMBell, BBertozzi-Villa, ABiryukov, SBolliger, ICharlson, FDavis, ADegenhardt, LDicker, DDuan, LErskine, HFeigin, VLFerrari, AJFitzmaurice, CFleming, TGraetz, NGuinovart, CHaagsma, JHansen, GMHanson, SWHeuton, KRHigashi, HKassebaum, NKyu, HLaurie, ELiang, XFLofgren, KLozano, RMacIntyre, MFMoradi-Lakeh, MNaghavi, MNguyen, GOdell, SOrtblad, KRoberts, DARoth, GASandar, LSerina, PTStanaway, JDSteiner, CThomas, BVollset, SEWhiteford, HWolock, TMYe, PPZhou, MGAvila, MAAasvang, GMAbbafati, COzgoren, AAAbd-Allah, FAziz, MIAAbera, SFAboyans, VAbraham, JPAbraham, BAbubakar, IAbu-Raddad, LJAbu-Rmeileh, NMEAburto, TCAchoki, TAckerman, INAdelekan, AAdemi, ZAdou, AKAdsuar, JCArnlov, JAgardh, EEAl Khabouri, MJAlam, SSAlasfoor, DAlbittar, MIAlegretti, MAAleman, AVAlemu, ZAAlfonso-Cristancho, RAlhabib, SAli, RAlla, FAllebeck, PAllen, PJAlMazroa, MAAlsharif, UAlvarez, EAlvis-Guzman, NAmeli, OAmini, HAmmar, WAnderson, BOAnderson, HRAntonio, CATAnwari, PApfel, HArsenijevic, VSAArtaman, AAsghar, RJAssadi, RAtkins, LSAtkinson, CBadawi, ABahit, MCBakfalouni, TBalakrishnan, KBalalla, SBanerjee, ABarker-Collo, SLBarquera, SBarregard, LBarrero, LHBasu, SBasu, ABaxter, ABeardsley, JBedi, NBeghi, EBekele, TBell, MLBenjet, CBennett, DABensenor, IMBenzian, HBernabe, EBeyene, TJBhala, NBhalla, ABhutta, ZQBienhoff, KBikbov, BBin Abdulhak, ABlore, JDBlyth, FMBohensky, MABasara, BBBorges, GBornstein, NMBose, DBoufous, SBourne, RRBoyers, LNBrainin, MBrauer, MBrayne, CEGBrazinova, ABreitborde, NJKBrenner, HBriggs, ADMBrooks, PMBrown, JBrugha, TSBuchbinder, RBuckle, GCBukhman, GBulloch, AGBurch, MBurnett, RCardenas, RCabral, NLNonato, IRCCampuzano, JCCarapetis, JRCarpenter, DOCaso, VCastaneda-Orjuela, CACatala-Lopez, FChadha, VKChang, JCChen, HLChen, WQChiang, PPChimed-Ochir, OChowdhury, RChristensen, HChristophi, CAChugh, SSCirillo, MCoggeshall, MCohen, AColistro, VColquhoun, SMContreras, AGCooper, LTCooper, CCooperrider, KCoresh, JCortinovis, MCriqui, MHCrump, JACuevas-Nasu, LDandona, RDandona, LDansereau, EDantes, HGDargan, PIDavey, GDavitoiu, DVDayama, ADe la Cruz-Gongora, Vde la Vega, SFDe Leo, Ddel Pozo-Cruz, BDellavalle, RPDeribe, KDerrett, SDes Jarlais, DCDessalegn, Mde Veber, GADharmaratne, SDDiaz-Torne, CDing, ELDokova, KDorsey, ERDriscoll, TRDuber, HDurrani, AMEdmond, KMEllenbogen, RGEndres, MErmakov, SPEshrati, BEsteghamati, AEstep, KFahimi, SFarzadfar, FFay, DFJFelson, DTFereshtehnejad, SMFernandes, JGFerri, CPFlaxman, AFoigt, NForeman, KJFowkes, FGRFranklin, RCFurst, TFutran, NDGabbe, BJGankpe, FGGarcia-Guerra, FAGeleijnse, JMGessner, BDGibney, KBGillum, RFGinawi, IAGiroud, MGiussani, GGoenka, SGoginashvili, KGona, Pde Cosio, TGGosselin, RAGotay, CCGoto, AGouda, HNGuerrant, RLGugnani, HCGunnell, DGupta, RGutierrez, RAHafezi-Nejad, NHagan, HHalasa, YHamadeh, RRHamavid, HHammami, MHankey, GJHao, YTHarb, HLHaro, JMHavmoeller, RHay, RJHay, SHedayati, MTPi, IBHHeydarpour, PHijar, MHoek, HWHoffman, HJHornberger, JCHosgood, HDHossain, MHotez, PJHoy, DGHsairi, MHu, HHu, GQHuang, JJHuang, CHuiart, LHusseini, AIannarone, MIburg, KMInnos, KInoue, MJacobsen, KHJassal, SKJeemon, PJensen, PNJha, VJiang, GJiang, YJonas, JBJoseph, JJuel, KKan, HDKarch, AKarimkhani, CKarthikeyan, GKatz, RKaul, AKawakami, NKazi, DSKemp, AHKengne, APKhader, YSKhalifa, SEAHKhan, EAKhan, GKhang, YHKhonelidze, IKieling, CKim, DKim, SKimokoti, RWKinfu, YKinge, JMKissela, BMKivipelto, MKnibbs, LKnudsen, AKKokubo, YKosen, SKramer, AKravchenko, MKrishnamurthi, RVKrishnaswami, SDefo, BKBicer, BKKuipers, EJKulkarni, VSKumar, KKumar, GAKwan, GFLai, TLalloo, RLam, HLan, QLansingh, VCLarson, HLarsson, ALawrynowicz, AEBLeasher, JLLee, JTLeigh, JLeung, RLevi, MLi, BLi, YCLi, YMLiang, JLim, SLin, HHLind, MLindsay, MPLipshultz, SELiu, SWLloyd, BKOhno, SLLogroscino, GLooker, KJLopez, ADLopez-Olmedo, NLortet-Tieulent, JLotufo, PALow, NLucas, RMLunevicius, RLyons, RAMa, JXMa, SMackay, MTMajdan, MMalekzadeh, RMapoma, CCMarcenes, WMarch, LMMargono, CMarks, GBMarzan, MBMasci, JRMason-Jones, AJMatzopoulos, RGMayosi, BMMazorodze, TTMcGill, NWMcGrath, JJMcKee, MMcLain, AMcMahon, BJMeaney, PAMehndiratta, MMMejia-Rodriguez, FMekonnen, WMelaku, YAMeltzer, MMemish, ZAMensah, GMeretoja, AMhimbira, FAMicha, RMiller, TRMills, EJMitchell, PBMock, CNMoffitt, TEIbrahim, NMMohammad, KAMokdad, AHMola, GLMonasta, LMontico, MMontine, TJMoore, ARMoran, AEMorawska, LMori, RMoschandreas, JMoturi, WNMoyer, MMozaffarian, DMueller, UOMukaigawara, MMurdoch, MEMurray, JMurthy, KSNaghavi, PNahas, ZNaheed, ANaidoo, KSNaldi, LNand, DNangia, VNarayan, KMVNash, DNejjari, CNeupane, SPNewman, LMNewton, CRNg, MNgalesoni, FNNhung, NTNisar, MINolte, SNorheim, OFNorman, RENorrving, BNyakarahuka, LOh, IHOhkubo, TOmer, SBOpio, JNOrtiz, APandian, JDPanelo, CIAPapachristou, CPark, EKParry, CDCaicedo, AJPPatten, SBPaul, VKPavlin, BIPearce, NPedraza, LSPellegrini, CAPereira, DMPerez-Ruiz, FPPerico, NPervaiz, APesudovs, KPeterson, CBPetzold, MPhillips, MRPhillips, DPhillips, BPiel, FBPlass, DPoenaru, DPolanczyk, GVPolinder, SPope, CAPopova, SPoulton, RGPourmalek, FPrabhakaran, DPrasad, NMQato, DQuistberg, DARafay, ARahimi, KRahimi-Movaghar, VRahman, SURaju, MRakovac, IRana, SMRazavi, HRefaat, ARehm, JRemuzzi, GResnikoff, SRibeiro, ALRiccio, PMRichardson, LRichardus, JHRiederer, AMRobinson, MRoca, ARodriguez, ARojas-Rueda, DRonfani, LRothenbacher, DRoy, NRuhago, GMSabin, NSacco, RLKsoreide, KSaha, SSahathevan, RSahraian, MASampson, USanabria, JRSanchez-Riera, LSantos, ISSatpathy, MSaunders, JESawhney, MSaylan, MIScarborough, PSchoettker, BSchneider, IJSchwebel, DCScott, JGSeedat, SSepanlou, SGSerdar, BServan-Mori, EEShackelford, KShaheen, AShahraz, SLevy, TSShangguan, SShe, JSheikhbahaei, SShepard, DSShi, PLShibuya, KShinohara, YShiri, RShishani, KShiue, IShrime, MGSigfusdottir, IDSilberberg, DHSimard, EPSindi, SSingh, JASingh, LSkirbekk, VSliwa, KSoljak, MSoneji, SSoshnikov, SSSpeyer, PSposato, LASreeramareddy, CTStoeckl, HStathopoulou, VKSteckling, NStein, MBStein, DJSteiner, TJStewart, AStork, EStovner, LJStroumpoulis, KSturua, LSunguya, BFSwaroop, MSykes, BLTabb, KMTakahashi, KTan, FTandon, NTanne, DTanner, MTavakkoli, MTaylor, HRAo, BJTTemesgen, AMTen Have, MTenkorang, EYTerkawi, ASTheadom, AMThomas, EThorne-Lyman, ALThrift, AGTleyjeh, IMTonelli, MTopouzis, FTowbin, JAToyoshima, HTraebert, JTran, BXTrasande, LTrillini, MTruelsen, TTrujillo, UTsilimbaris, MTuzcu, EMUkwaja, KNUndurraga, EAUzun, SBvan Brakel, WHde Vijver, SVVan Dingenen, Rvan Gool, CHVarakin, YYVasankari, TJVavilala, MSVeerman, LJVelasquez-Melendez, GVenketasubramanian, NVijayakumar, LVillalpando, SViolante, FSVlassov, VVWaller, SWallin, MTWan, XWang, LHWang, JLWang, YPWarouw, TSWeichenthal, SWeiderpass, EWeintraub, RGWerdecker, AWessells, KRRWesterman, RWilkinson, JDWilliams, HCWilliams, TNWoldeyohannes, SMWolfe, CDAWong, JQWong, HDWoolf, ADWright, JLWurtz, BXu, GLYang, GHYano, YYenesew, MAYentur, GKYip, PYonemoto, NYoon, SJYounis, MYu, CHKim, KYZaki, MESZhang, YZhao, ZZhao, YZhu, JZonies, DZunt, JRSalomon, JAMurray, CJL
Lancet (London, England). 386(9995):743-800
Academic Journal
Nursing Clinics of North America (NURS CLIN NORTH AM), 1966 Jun; 1: 275-275. (1p)
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
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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