학술논문

발행년
-
(예 : 2010-2015)
'학술논문' 에서 검색결과 120건 | 목록 1~10
Academic Journal
O'Donnell-Luria, AHPais, LSFaundes, VWood, JCSveden, ALuria, VAbou Jamra, RAccogli, AAmburgey, KAnderlid, BMAzzarello-Burri, SBasinger, AABianchini, CBird, LMBuchert, RCarre, WCeulemans, SCharles, PCox, HCulliton, LCurro, ADemurger, FDowling, JJDuban-Bedu, BDubourg, CEiset, SEEscobar, LFFerrarini, AHaack, TBHashim, MHeide, SHelbig, KLHelbig, IHeredia, RHeron, DIsidor, BJonasson, ARJoset, PKeren, BKok, FKroes, HYLavillaureix, ALu, XMaas, SMMaegawa, GHBMarcelis, CLMMark, PRMasruha, MRMcLaughlin, HMMcWalter, KMelchinger, EUMercimek-Andrews, SNava, CPendziwiat, MPerson, RRamelli, GPRamos, LLPRauch, AReavey, CRenieri, ARiess, ASanchez-Valle, ASattar, SSaunders, CSchwarz, NSmol, TSrour, MSteindl, KSyrbe, STaylor, JCTelegrafi, AThiffault, ITrauner, DAvan der Linden, Hvan Koningsbruggen, SVillard, LVogel, IVogt, JWeber, YGWentzensen, IMWidjaja, EZak, JBaxter, SBanka, SRodan, LHMcrae, JFClayton, SFitzgerald, TWKaplanis, JPrigmore, ERajan, DSifrim, AAitken, SAkawi, NAlvi, MAmbridge, KBarrett, DMBayzetinova, TJones, PJones, WDKing, DKrishnappa, NMason, LESingh, TTivey, ARAhmed, MAnjum, UArcher, HArmstrong, RAwada, JBalasubramanian, MBaralle, DBarnicoat, ABatstone, PBaty, DBennett, CBerg, JBernhard, BBevan, APBitner-Glindzicz, MBlair, EBlyth, MBohanna, DBourdon, LBourn, DBradley, LBrady, ABrent, SBrewer, CBrunstrom, KBunyan, DJBurn, JCanham, NCastle, BChandler, KChatzimichali, ECilliers, DClarke, AClasper, SClayton-Smith, JClowes, VCoates, ACole, TColgiu, ICollins, ACollinson, MNConnell, FCooper, NCresswell, LCross, GCrow, YD'Alessandro, MDabir, TDavidson, RDavies, Sde Vries, DDean, JDeshpande, CDevlin, GDixit, ADobbie, ADonaldson, ADonnai, DDonnelly, DDonnelly, CDouglas, ADouzgou, SDuncan, AEason, JEllard, SEllis, IElmslie, FEvans, KEverest, SFendick, TFisher, RFlinter, FFoulds, NFry, AFryer, AGardiner, CGaunt, LGhali, NGibbons, RGill, HGoodship, JGoudie, DGray, EGreen, AGreene, PGreenhalgh, LGribble, SHarrison, RHarrison, LHarrison, VHawkins, RHe, LHellens, SHenderson, AHewitt, SHildyard, LHobson, EHolden, SHolder, MHolder, SHollingsworth, GHomfray, THumphreys, MHurst, JHutton, BIngram, SIrving, MIslam, LJackson, AJarvis, JJenkins, LJohnson, DJones, EJosifova, DJoss, SKaemba, BKazembe, SKelsell, RKerr, BKingston, HKini, UKinning, EKirby, GKirk, CKivuva, EKraus, AKumar, DKumar, VKALachlan, KLam, WLampe, ALangman, CLees, MLim, DLongman, CLowther, GLynch, SAMagee, AMaher, EMale, AMansour, SMarks, KMartin, KMaye, UMcCann, EMcConnell, VMcEntagart, MMcGowan, RMckay, KMckee, SMcMullan, DJMcNerlan, SMcWilliam, CMehta, SMetcalfe, KMiddleton, AMiedzybrodzka, ZMiles, EMohammed, SMontgomery, TMoore, DMorgan, SMorton, JMugalaasi, HMurday, VMurphy, HNaik, SNemeth, ANevitt, LNewbury-Ecob, RNorman, AO'Shea, ROgilvie, COng, KRPark, SMParker, MJPatel, CPaterson, JPayne, SPerrett, DPhipps, JPilz, DTPollard, MPottinger, CPoulton, JPratt, NPrescott, KPrice, SPridham, AProcter, APurnell, HQuarrell, ORagge, NRahbari, RRandall, JRankin, JRaymond, LRice, DRobert, LRoberts, ERoberts, JRoberts, PRoberts, GRoss, ARosser, ESaggar, ASamant, SSampson, JSandford, RSarkar, ASchweiger, SScott, RScurr, ISelby, ASeller, ASequeira, CShannon, NSharif, SShaw-Smith, CShearing, EShears, DSheridan, ESimonic, ISingzon, RSkitt, ZSmith, ASmith, KSmithson, SSneddon, LSplitt, MSquires, MStewart, FStewart, HStraub, VSuri, MSutton, VSwaminathan, GJSweeney, ETatton-Brown, KTaylor, CTaylor, RTein, MTemple, IKThomson, JTischkowitz, MTomkins, STorokwa, ATreacy, BTurner, CTurnpenny, PTysoe, CVandersteen, AVarghese, VVasudevan, PVijayarangakannan, PWakeling, EWallwark, SWaters, JWeber, AWellesley, DWhiteford, MWidaa, SWilcox, SWilkinson, EWilliams, DWilliams, NWilson, LWoods, GWragg, CWright, MYates, LYau, MNellaker, CParker, MFirth, HVWright, CFFitzPatrick, DRBarrett, JCHurles, ME
American journal of human genetics. 104(6):1210-1222
Academic Journal
Jacquemont, SReymond, AZufferey, FHarewood, LWalters, RGKutalik, ZMartinet, DShen, YPValsesia, ABeckmann, NDThorleifsson, GBelfiore, MBouquillon, SCampion, Dde Leeuw, Nde Vries, BBAEsko, TFernandez, BAFernandez-Aranda, FFernandez-Real, JMGratacos, MGuilmatre, AHoyer, JJarvelin, MRKooy, RFKurg, ALe Caignec, CMannik, KPlatt, OSSanlaville, DVan Haelst, MMGomez, SVWalha, FWu, BLYu, YGAboura, AAddor, MCAlembik, YAntonarakis, SEArveiler, BBarth, MBednarek, NBena, FBergmann, SBeri, MBernardini, LBlaumeiser, BBonneau, DBottani, ABoute, OBrunner, HGCailley, DCallier, PChiesa, JChrast, JCoin, LCoutton, CCuisset, JMCuvellier, JCDavid, Ade Freminville, BDelobel, BDelrue, MADemeer, BDescamps, DDidelot, GDieterich, KDisciglio, VDoco-Fenzy, MDrunat, SDuban-Bedu, BDubourg, CMoustafa, JSEElliott, PFaas, BHWFaivre, LFaudet, AFellmann, FFerrarini, AFisher, RFlori, EForer, LGaillard, DGerard, MGieger, CGimelli, SGimelli, GGrabe, HJGuichet, AGuillin, OHartikainen, ALHeron, DHippolyte, LHolder, MHomuth, GIsidor, BJaillard, SJaros, ZJimenez-Murcia, SHelas, GJJonveaux, PKaksonen, SKeren, BKloss-Brandstatter, AKnoers, NVAMKoolen, DAKroisel, PMKronenberg, FLabalme, ALandais, ELapi, ELayet, VLegallic, SLeheup, BLeube, BLewis, SLucas, JMacDermot, KDMagnusson, PMarshall, CMathieu-Dramard, MMcCarthy, MIMeitinger, TMencarelli, MAMerla, GMoerman, AMooser, VMorice-Picard, FMucciolo, MNauck, MNdiaye, NCNordgren, APasquier, LPetit, FPfundt, RPlessis, GRajcan-Separovic, ERamelli, GPRauch, ARavazzolo, RReis, ARenieri, ARichart, CRied, JSRieubland, CRoberts, WRoetzer, KMRooryck, CRossi, MSaemundsen, ESatre, VSchurmann, CSigurdsson, EStavropoulos, DJStefansson, HTengstrom, CThorsteinsdottir, UTinahones, FJTouraine, RVallee, Lvan Binsbergen, EVan der Aa, NVincent-Delorme, CVisvikis-Siest, SVollenweider, PVolzke, HVulto-van Silfhout, ATWaeber, GWallgren-Pettersson, CWitwicki, RMZwolinksi, SAndrieux, JEstivill, XGusella, JFGustafsson, OMetspalu, AScherer, SWStefansson, KBlakemore, AIFBeckmann, JSFroguel, P
Nature. 478(7367):97-U111
Academic Journal
Marsaud, CélineRossignol, SylvieTounian, PatrickNetchine, IrèneDubern, BéatriceAbadie, VAlcayde, SAlembik, YAmiel, JBaujat, GBaumann-Morel, CBieth, EBertrand, AMBonneau, DBouhours Nouet, NBrachet, CBrioude, FBrossier, JPBoute, OCabrol, SCarel, JCChabrol, BChivu, OChristin, PCollignon, PCordier, MPCormier Daire, VCoubes, CCoupe, BCoutant, RCraen, MCrosnier, HDe Baufort, CDavid, ADelahaye, ADelobel, BDelrue, MADieux Coeslier, ADommergues, MADoray, BDuban-Bedu, BDufresne, SEdery, PEsteva, BFarges, CFechtner, IFrancannet, CGilbert Dussardier, BGilbert, BGinglinger, EGiullano, FGoldenberg, AHamiel, OHarbison, MDHeinrichs, CHeron, DHolder, MHouang, MGenevieve, DGerard, MGonzales, MJantchou, PJonveaux, PJouk, PSKurtz, FLe Bouc, YLe Merrer, MLinglart, ALeheup, BLebrun, MLeger, JLeinhart, ALoeuille, GAManouvrier, SMartin-Coignard, DMas, JCMathieu, MMercier, SMignot, BMorice-Picard, FMorin, GNewfield, ROdent, SOliver-Petit, IOlivier-Faivre, LPetriczko, EPhilip, NPienkowski, CPinson, LPinto, GPolak, MQuelin, CPort-lis, MReiter, JCRio, MRiviere, MFRoquelaure, BSalem, JSimon, DSoskin, SSznajer, YTauber, MThauvin, CTouraine, RTeinturier, CToutain, AVan Maldergem, LVerloes, AVincent Delorme, CVu-Hong, T-AWeill, J
Archives of Disease in Childhood. Apr 01, 2015 100(4):353-358
Academic Journal
Leitão E; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Schröder C; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Parenti I; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Dalle C; Institut du Cerveau et de la Moelle épinière (ICM), Sorbonne Université, UMR S 1127, Inserm U1127, CNRS UMR 7225, F-75013, Paris, France.; Rastetter A; Institut du Cerveau et de la Moelle épinière (ICM), Sorbonne Université, UMR S 1127, Inserm U1127, CNRS UMR 7225, F-75013, Paris, France.; Kühnel T; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Kuechler A; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Kaya S; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Gérard B; Unité de Génétique Moléculaire, IGMA, Hôpitaux Universitaire de Strasbourg, Strasbourg, France.; Schaefer E; Service de Génétique Médicale, IGMA, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Nava C; Institut du Cerveau et de la Moelle épinière (ICM), Sorbonne Université, UMR S 1127, Inserm U1127, CNRS UMR 7225, F-75013, Paris, France.; Drouot N; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, 67400, France.; Centre National de la Recherche Scientifique, UMR7104, Illkirch, 67400, France.; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, 67400, France.; Université de Strasbourg, Illkirch, 67400, France.; Engel C; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, 67400, France.; Centre National de la Recherche Scientifique, UMR7104, Illkirch, 67400, France.; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, 67400, France.; Université de Strasbourg, Illkirch, 67400, France.; Piard J; Centre de Génétique Humaine, CHU Besançon, Besançon, France.; INSERM UMR1231, Equipe Génétique des Anomalies du Développement, Université de Bourgogne-Franche-Comté, Dijon, France.; Duban-Bedu B; Centre de génétique chromosomique, Hôpital Saint-Vincent de Paul, Lille, France.; Villard L; Aix-Marseille University, INSERM, MMG, UMR-S 1251, Faculté de médecine, Marseille, France.; Département de Génétique Médicale, APHM, Hôpital d'Enfants de La Timone, Marseille, France.; Stegmann APA; Department of Human Genetics, Radboud University Medical Center, 6500 HB, Nijmegen, The Netherlands.; Department of Clinical Genetics, Maastricht University Medical Center+, Maastricht, The Netherlands.; Vanhoutte EK; Department of Clinical Genetics, Maastricht University Medical Center+, Maastricht, The Netherlands.; Verdonschot JAJ; Department of Clinical Genetics, Maastricht University Medical Center+, Maastricht, The Netherlands.; Cardiovascular Research Institute (CARIM), Departments of Cardiology, Maastricht University Medical Center, Maastricht, The Netherlands.; Kaiser FJ; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Tran Mau-Them F; INSERM UMR1231, Equipe Génétique des Anomalies du Développement, Université de Bourgogne-Franche-Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France.; Scala M; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 16132, Genoa, Italy.; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, 16147, Genoa, Italy.; Striano P; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 16132, Genoa, Italy.; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, 16147, Genoa, Italy.; Frints SGM; Department of Clinical Genetics, Maastricht University Medical Center+, Maastricht, The Netherlands.; Department of Genetics and Cell Biology, Faculty of Health Medicine Life Sciences, Maastricht University Medical Center+, Maastricht University, Maastricht, The Netherlands.; Argilli E; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.; Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.; Sherr EH; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.; Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.; Elder F; UF de Génomique du Développement, Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, APHP-Sorbonne Université, Paris, France.; Buratti J; UF de Génomique du Développement, Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, APHP-Sorbonne Université, Paris, France.; Keren B; UF de Génomique du Développement, Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, APHP-Sorbonne Université, Paris, France.; Mignot C; Institut du Cerveau et de la Moelle épinière (ICM), Sorbonne Université, UMR S 1127, Inserm U1127, CNRS UMR 7225, F-75013, Paris, France.; APHP, Sorbonne Université, Département de Génétique, Centre de Référence Déficiences Intellectuelles de Causes Rares, Groupe Hospitalier Pitié-Salpêtrière and Hôpital Trousseau, Paris, France.; Héron D; APHP, Sorbonne Université, Département de Génétique, Centre de Référence Déficiences Intellectuelles de Causes Rares, Groupe Hospitalier Pitié-Salpêtrière and Hôpital Trousseau, Paris, France.; Mandel JL; Unité de Génétique Moléculaire, IGMA, Hôpitaux Universitaire de Strasbourg, Strasbourg, France.; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, 67400, France.; Centre National de la Recherche Scientifique, UMR7104, Illkirch, 67400, France.; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, 67400, France.; Université de Strasbourg, Illkirch, 67400, France.; Gecz J; School of Medicine, The University of Adelaide, Adelaide, 5005, SA, Australia.; Robinson Research Institute, The University of Adelaide, Adelaide, SA, 5006, Australia.; South Australian Health and Medical Research Institute, The University of Adelaide, Adelaide, 5005, SA, Australia.; Kalscheuer VM; Research Group Development and Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany.; Horsthemke B; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Piton A; Unité de Génétique Moléculaire, IGMA, Hôpitaux Universitaire de Strasbourg, Strasbourg, France.; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, 67400, France.; Centre National de la Recherche Scientifique, UMR7104, Illkirch, 67400, France.; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, 67400, France.; Université de Strasbourg, Illkirch, 67400, France.; Depienne C; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany. christel.depienne@uni-due.de.
Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Academic Journal
Jouret G; Laboratoire national de santé (LNS), National Center of Genetics (NCG), Dudelange, Luxembourg.; Heide S; Service de Génétique Cytogénétique, Embryologie Hôpital Pitié-Salpétrière, France.; Sorlin A; Laboratoire national de santé (LNS), National Center of Genetics (NCG), Dudelange, Luxembourg.; Centre de Génétique, CHU de Dijon, Dijon, France.; Génétique des Anomalies du Développement, Inserm 1231 GAD, Université de Bourgogne, France.; Faivre L; Centre de Génétique, CHU de Dijon, Dijon, France.; Génétique des Anomalies du Développement, Inserm 1231 GAD, Université de Bourgogne, France.; Chantot-Bastaraud S; Service de Génétique Et Embryologie Médicales, CHU Paris Est, Hôpital d'Enfants Armand-Trousseau, France.; Beneteau C; Service de Génétique Médicale, CHU de Nantes, Institut de Biologie, France.; Denis-Musquer M; Service d'Anatomie et Cytologie Pathologiques, Hôpital-Dieu, Nantes, France.; Turnpenny PD; Clinical Genetics Department, Royal Devon and Exeter Hospital, UK.; Coutton C; Service de Génétique Médicale, Grenoble, France.; Vieville G; Service de Génétique Médicale, Grenoble, France.; Thevenon J; Service de Génétique Médicale, Grenoble, France.; Larson A; Clinical Genetics Department, Children's Hospital Colorado, Littleton, Colorado, USA.; Petit F; Clinique de Génétique 'Guy Fontaine', CHU de Lille, France.; Boudry E; Institut de Génétique Médicale, CHU de Lille, France.; Smol T; Institut de Génétique Médicale, CHU de Lille, France.; Delobel B; Centre de Génétique Chromosomique, GH de l'Institut, Catholique de Lille, France.; Duban-Bedu B; Centre de Génétique Chromosomique, GH de l'Institut, Catholique de Lille, France.; Fallerini C; Medical Genetics Department, University of Siena, Siena, Italy.; Mari F; Medical Genetics Department, University of Siena, Siena, Italy.; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.; Lo Rizzo C; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.; Renieri A; Medical Genetics Department, University of Siena, Siena, Italy.; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.; Caberg JH; Centre de Génétique Humaine, CHU de Liège, Liège, Belgium.; Denommé-Pichon AS; Centre de Génétique, CHU de Dijon, Dijon, France.; UF6254 Innovation en Diagnostic Genomique des Maladies Rares, Dijon, France.; Tran Mau-Them F; Centre de Génétique, CHU de Dijon, Dijon, France.; UF6254 Innovation en Diagnostic Genomique des Maladies Rares, Dijon, France.; Maystadt I; Centre de Genetique Humaine, Institut de Pathologie et de Genetique, Charleroi, Belgium.; Courtin T; Département de génétique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, France.; Keren B; Département de génétique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, France.; Mouthon L; Département de génétique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, France.; Charles P; Département de génétique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, France.; Cuinat S; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, France.; Isidor B; Service de Génétique Médicale, Centre Hospitalier Universitaire de Nantes, France.; Theis P; Laboratoire national de santé (LNS), National Center of Genetics (NCG), Dudelange, Luxembourg.; Müller C; Laboratoire national de santé (LNS), National Center of Genetics (NCG), Dudelange, Luxembourg.; Kulisic M; Laboratoire national de santé (LNS), National Center of Genetics (NCG), Dudelange, Luxembourg.; Türkmen S; Laboratoire national de santé (LNS), National Center of Genetics (NCG), Dudelange, Luxembourg.; Stieber D; Laboratoire national de santé (LNS), National Center of Genetics (NCG), Dudelange, Luxembourg.; Bourgeois D; Laboratoire national de santé (LNS), National Center of Genetics (NCG), Dudelange, Luxembourg.; Scalais E; Pediatric Neurology Unit, Pediatric Department, Centre Hospitalier de Luxembourg, Luxembourg City, Luxembourg.; Klink B; Laboratoire national de santé (LNS), National Center of Genetics (NCG), Dudelange, Luxembourg.
Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Academic Journal
Loviglio, M NLeleu, MMännik, KPasseggeri, MGiannuzzi, Gvan der Werf, IWaszak, S MZazhytska, MRoberts-Caldeira, IGheldof, NMigliavacca, EAlfaiz, A AHippolyte, LMaillard, A MLoviglio, Maria NiclaMännik, Katrinvan der Werf, IlseGiannuzzi, GiulianaZazhytska, MariannaGheldof, NeleMigliavacca, EugeniaAlfaiz, Ali ARoberts-Caldeira, InêsHippolyte, LoyseMaillard, Anne MFerrarini, AlessandraButschi, Florence NielConrad, BernardAddor, Marie-ClaudeBelfiore, MarcoRoetzer, KatharinaDijck, Anke VanBlaumeiser, BettinaKooy, FrankRoelens, FilipDheedene, AnneliesChiaie, Barbara DelleMenten, BjörnOostra, AnnCaberg, Jean-HubertCarter, MelissaKellam, BarbaraStavropoulos, Dimitri JMarshall, ChristianScherer, Stephen WWeksberg, RosannaCytrynbaum, CherylBassett, AnneLowther, ChelseaGillis, JaneMacKay, SaraBache, IbenOusager, Lilian BSmerdel, Maja PatriciaGraakjaer, JesperKjaergaard, SusanneMetspalu, AndresMathieu, MicheleBonneau, DominiqueGuichet, AgnesParent, PhilippeFérec, ClaudeGerard, MarionPlessis, GhislaineLespinasse, JamesMasurel, AliceMarle, NathalieFaivre, LaurenceCallier, PatrickLayet, ValerieMeur, Nathalie LeLe Goff, CélineDuban-Bedu, BénédicteSukno, SylvieBoute, OdileAndrieux, JorisBlanchet, PatriciaGeneviève, DavidPuechberty, JacquesSchneider, AnouckLeheup, BrunoJonveaux, PhilippeMercier, SandraDavid, AlbertLe Caignec, Cédricde Pontual, LoicPipiras, EvaJacquette, AureliaKeren, BorisGilbert-Dussardier, BrigitteBilan, FredericGoldenberg, AliceChambon, PascalToutain, AnnickTill, MarianneSanlaville, DamienLeube, BarbaraRoyer-Pokora, BrigitteGrabe, Hans JörgenSchmidt, Carsten OliverSchurmann, ClaudiaHomuth, GeorgThorleifsson, GudmarThorsteinsdottir, UnnurBernardini, LauraNovelli, AntonioMicale, LuciaMerla, GiuseppeZollino, MarcellaMari, FrancescaRizzo, Caterina LoRenieri, AlessandraSilengo, MargheritaVulto-van Silfhout, Anneke TSchouten, MeykePfundt, Rolphde Leeuw, NicoleVansenne, FleurMaas, Saskia MBarge-Schaapveld, Daniela QCMKnegt, Alida CStadheim, BarbroRodningen, OlaugHouge, GunnarPrice, SueHawkes, LaraCampbell, CarolynKini, UshaVogt, JulieWalters, RobinBlakemore, AlexandraGusella, James FShen, YipingScott, DarylBacino, Carlos ATsuchiya, KarenLadda, RogerSell, SusanAsamoah, AlexanderHamati, Aline IRosenfeld, Jill AShaffer, Lisa GMitchell, ElyseHodge, Jennelle CBeckmann, Jacques SJacquemont, SébastienReymond, AlexandreEwans, Lisa JMowat, DavidWalker, JanAmor, David JEsch, Hilde VanLeroy, PatriciaBamforth, John-StevenBabu, DeeptiIsidor, BertrandDiDonato, NataliyaHackmann, KarlPasseggeri, MarziaHaeringen, Arie vanSmith, RosemarieEllingwood, SaraFarber, Darren MPuri, VinayZadeh, NedaWeaver, David DMiller, MandyWilks, TimothyJorgez, Carolina JLafayette, DeeDeeVan Dijck, AKooy, R FSanlaville, DRosenfeld, J AShaffer, L GAndrieux, JMarshall, CScherer, S WShen, YGusella, J FThorsteinsdottir, UThorleifsson, GDermitzakis, E TDeplancke, BBeckmann, J SRougemont, JJacquemont, SReymond, A
Molecular Psychiatry. June 2017, Vol. 22 Issue 6, 836
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[검색어] Duban-Bedu, B
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