학술논문

발행년
-
(예 : 2010-2015)
'학술논문' 에서 검색결과 34건 | 목록 1~10
Academic Journal
Braisch, UMuche, RRothenbacher, DLandwehrmeyer, GBLong, JDOrth, MBachoud-Levi, ACBentivoglio, ARBiunno, IBonelli, RMBurgunder, JMDunnett, SBFerreira, JJHandley, OJHeiberg, AIllmann, TLevey, JRamos-Arroyo, MNielsen, JEKoivisto, SPPaivarinta, MRoos, RACSebastian, ARTabrizi, SJVandenberghe, WVerellen-Dumoulin, CUhrova, TWahlstrom, JZaremba, JBaake, VBarth, KBos, RCome, AGuedes, LCFinisterra, AMGarde, MBBetz, SCallaghan, JCapodarca, SWildson, SCda Silva, VDi Renzo, MEcker, DFinisterra, MFullam, RGenoves, CGilling, MHvalstedt, CHeld, CKoppers, KLamanna, CLaura, MDescals, AMMartinez-Horta, SMestre, TMinster, SMonza, DMutze, LOehmen, MPadieu, HPaterski, LPeppa, NRindal, BRoren, NSasinkova, PSeliverstov, YTimewell, ETownhill, JCubillo, PTvan Walsem, MRWitjes-Ane, MNWitkowski, GWright, AYudina, EZielonka, DZielonka, EZinzi, PBraunwarth, EMBrugger, FBuratti, LHametner, EMHepperger, CHolas, CHotter, AHussl, ALarcher, BMahlknecht, PMuller, CPinter, BPoewe, WSeppi, KSprenger, FWenning, GDupuis, MMinet, CRibai, PVan Paemel, DKlempir, JMajerova, VRoth, JBabiloni, BDebruxelles, SDuche, CGoizet, CJameau, LLafoucriere, DSpampinato, UBoisse, MFde Langavant, LCLemoine, LMorgado, GYoussov, KAnnic, ABarthelemy, RDe Bruycker, CCabaret, MCarette, ASCarriere, NDecorte, EDefebvre, LDelliaux, MDelval, ADepelchin, ADestee, ADewulf-Pasz, NDondaine, TDugauquier, FDujardin, KKrystkowiak, PLemaire, MHManouvrier, SPeter, MPlomhause, LSablonniere, BSimonin, CTard, CThibault-Tanchou, SVuillaume, IBellonet, MBenoit, ABlin, SCourtin, FDuru, CFasquel, VGodefroy, OMantaux, BRoussel, MTir, MSchuler, BWannepain, SAzulay, JPChabot, CDelfini, MEusebio, AFluchere, FGrosjean, HMundler, LNowak, MBioux, SBliaux, EGirard, CGuyant-Marechal, LHannequin, DHannier, VJourdain, SMaltete, DPouliquen, DBlondeau, LCalvas, FCheriet, SDelabaere, HDemonet, JFPariente, JPierre, MBeuth, MGelderblom, HPriller, JPruss, HSpruth, EThiel, SEllrichmannberlin, GHerrmann, LHoffmann, RKaminski, BSaft, CBosredon, CHunger, ULohle, MMaass, AOssig, CSchmidt, SStorch, AWolz, AWolz, MKohl, ZKozay, CUllah, JWinkler, JBergmann, UBoringer, RCapetian, PKammel, GLambeck, JMeier, SRijntjes, MZucker, BBoelmans, KGanos, CGoerendt, IHeinicke, WHidding, ULewerenz, JMunchau, ASchmalfeld, JStubbe, LZittel, SDiercks, GDressler, DFrancis, FGayde-Stephan, SGorzolla, HKramer, BMinschke, RSchrader, CTacik, PLonginus, BLusebrink, AMuhlau, MPeinemann, AStadtler, MWeindl, AWinkelmann, JZiegler, CBechtel, NBeckmann, HBohlen, SGopfert, NHolzner, ELange, HReilmann, RRohm, SRumpf, SSass, CSchepers, SWeber, NBuck, AConnemann, JGeitner, CKesse, ALandwehrmeyer, BLezius, FNepper, SNiess, ASchneider, ASchwenk, DSussmuth, STrautmann, SWeydt, PKlebe, SMusacchio, TLeypold, CNoth, KCormio, Cde Tommaso, MFranco, GSciruicchio, VSerpino, CCalandra-Buonaura, GCapellari, SCortelli, PGallassi, RPoda, RSambati, LScaglione, CMaserati, MSAgosti, CBarlati, SCompostella, SMarchina, EPadovani, ABertini, EGhelli, EGinestroni, AMechi, CPaganini, MPiacentini, SPradella, SRomoli, AMSorbi, SAbbruzzese, Gdi Poggio, MBFerrandes, GMandich, PMarchese, RTamburini, Tvan den Bogaard, SJADumas, EMt'Hart, EPKampstra, ASchoonderbeek, AAaserud, OBjorgo, KBorgeod, NDramstad, EFannemel, MFrich, JCGorvell, PFLorentzen, ERetterstol, LRosby, OSikiric, AStokke, Bvan Walsem, MWehus, RBjornevoll, ISando, SBHaug, MGStorseth, HHArntsen, VDziadkiewicz, AKonkel, ANarozanska, ERobowski, PSitek, ESlawek, JSoltan, WSzinwelski, MArkuszewski, MBlaszczyk, MBoczarska-Jedynak, MCiach-Wysocka, EGorzkowska, ANska-Myga, BJKaczmarczyk, AKlodowska-Duda, GOpala, GRudzinska, MStompel, DBanaszkiewicz, KBocwinska, DBojakowska-Jaremek, KDec, MGrabska, NKrawczyk, GMKubowicz, EMalec-Litwinowicz, MStenwak, ASzczudlik, ASzczygiel, EWojcik, MWasielewska, ABryl, JAACiesielska, AKlimberg, AMarcinkowski, JSamara, HSempolowicz, JSniewski, BWGogol, AJanik, PJamrozik, ZKaminska, AKwiecinski, HAntczak, JJachinska, KKrysa, WRakowicz, MRichter, PRola, RRyglewicz, DSienkiewicz-Jarosz, HStepniak, ISulek, AZdzienicka, EZiora-Jakutowicz, KJanuario, CJulio, FCoelho, MMendes, TRosa, MMValadas, AKopishinskaya, SKorotysh, MHerrera, CDMoreno, PGBas, JBusquets, NCalopa, MClassen, SJDedicha, NRBuongiorno, MTMaria, ADSMunoz, ESantacruz, PBarbera, MAPardo, SAGuia, DBCalzado, NHernanz, LCDiaz-Zorita, JPTCatena, JLFerrer, PQCarruesco, GTRobert, MFViladrich, CMRoca, EIdiago, JMRRiballo, AVCampolongo, Ade Bobadilla, RFBojarsky, JKPagonabarraga, JPerez, JPRibosa, RVilla, CGil, MAACorrales, KBEsteban, JCGGonzalez, AMerino, BTCubo, EPolo, CGMariscal, NRomero, SGArbelo, JMde Molina, RMMartin, IPerianez, JMUdaeta, BAlonso-Frech, FFrades, BVillanueva, MASevilla, MAZFrech, FAFenollar, MDGarcia, RGRVillanueva, CBascunana, MVentura, MFRibas, GGde Yebenes, JGMoreno, JLLSBarral, VMRuiz, PJGGarcia, ALopez, RGBarcenas, AHMartinez-Descals, AMartin, VPMartinez, NRArtiga, MJSSanchez, VPueyo, AGonzalez, SGuisasola, LMRibacoba, MPPRSalvador, CLozano, PSCaldentey, JGRamirez, ILArques, PNLopera, MRPastor, BVGaston, IGarcia-Amigot, FMartinez-Jaurrieta, MDRamos-Arroyo, MACarrillo, FRedondo, MTCMir, PGonzalez, LVMoreno, JMGLucena, CMPena, JCRedondo, LSanchez, VSFernandez, CMMata, MPLemos, MDRBosca, MBurguera, JAVilaplana, FCBCPSolis, PFiguerola, BJPalanca, PMBerglund, PConstantinescu, RFredlund, GHosterey-Ugander, ULinnsand, PNeleborn-Lingefjard, LPalhagen, SSvenningsson, PPaucar, MWallden, TEkwall, CGoller, MLSundblom, JStebler, YKaelin, ARomero, ISchupbach, MZaugg, SWJung, HPetersen, JAuer, MMihaylova, VVernon, NAkhtar, SCrooks, JCurtis, Ade Souza, JPiedad, JRickards, HWright, JColeman, CCraven, JHaig-Brown, DPallett, ASimpson, SWeekes, RCoulthard, EGethin, LHayward, BSieradzan, KBusse, MButcher, CDunnett, SClenaghan, CHunt, SJones, LJones, UKhalil, HOwen, MPrice, KRosser, AEdwards, MHo, CMcGill, MPorteous, MPearson, PHarrower, TIrvine, SBrockie, PFoster, JJohns, NMcKenzie, SRothery, JThomas, GYates, SDeith, CIreland, JRitchie, SAndrew, AFrost, JNoad, RCosgrove, JGallantree, DHamer, SHobson, EJamieson, SKraus, ALongthorpe, MMarkova, IMusgrave, HPeacy, CRaman, ARowett, LToscano, JWild, SYardumian, PClayton, CDipple, HFreire-Patino, DHallam, CMiddleton, JAlusi, SDavies, RFoy, KGerrans, ELeggett, HPate, LAnjum, UCoebergh, JEddy, CLahiri, NMcEntagart, MPatton, MPeterson, MRose, SAndrews, TBrown, SBruno, SChu, EDoherty, KGolding, CHaider, SHensman, DLewis, MNovak, MPatel, ARobertson, NRosser, ETabrizi, STaylor, RWarner, TWild, EArran, NBek, JCraufurd, DHare, MHoward, LHuson, SJohnson, LJones, MKrishnamoorthy, AMurphy, HOughton, EPartington-Jones, LRogers, DSollom, ASnowden, JStopford, CThompson, JTinkler, PTrender-Gerhard, IVerstraelen, NWestmoreland, LCass, GDavidson, LDavison, JFullerton, NHolmes, KKomati, SMcDonnell, SMohammed, ZMorgan, KSavage, LSingh, BWood, JKnight, CO'Neill, MDas Purkayastha, DNemeth, AHSiuda, GValentine, RDixon, KArmstrong, RHarrison, DHughes, MLarge, SDonovan, JOPalmer, AParkinson, ASoltysiak, BTimings, LWilliams, JBurn, JBailey, WMajeed, TBandmann, OBradbury, AFairtlough, HFillingham, KFoustanos, IGill, PKazoka, MO'Donovan, KNevitt, LQuarrell, OTaylor, CTidswell, KAgarwal, VAnderson, MGunner, KHarris, KHayward, EHeywood, MKeys, LKipps, CMacKinnon, LSmalley, SGowers, LPowell, KBethwaite, PEdwards, RFuller, KPhillips, MTan, LLau, PNPica, EShoulson, IGusella, JGForoud, TAntonijevic, Ivankammen, DDorsey, RWarner, JGiuliano, JVetter, LSuchowersky, OBeck, COakes, DMarshall, FMarder, KFrucht, SMoskowitz, CClouse, RWasserman, PShannon, KJaglin, JJankovic, JPalao, AHarrison, MSinger, CQuesada, MHersch, SRosas, DTanev, KMalarick, KColcher, ASanchez-Ramos, JKostyk, SPaulsen, JPerlmutter, JTabbal, SRoss, CNucifora, FDubinsky, RDubinsky, HKlimek, MLJones, RTesta, CMorgan, JMohlo, EKang, UAgarwal, PFactor, SJennings, DHiggins, DAdams, JFrank, SSaint-Hilaire, MDiggin, MFurtado, SWalker, FO'Neill, CHunt, VQuaid, KLeDoux, MRaymond, LLeavitt, BDecolongon, JPerlman, SPeavy, GGoldstein, JKumar, RMcCusker, EGriffith, JLoy, CWheelock, VTempkin, TMartin, ANance, MMallonee, WSuter, GRevilla, FGartner, MDrazinic, CFitzpatrick, MJPanisset, MDuff, KScott, BWeiner, WRobottom, BChiu, EYastrubetskaya, OChurchyard, AGreenamyre, TJRobertson, SEaton, KLindsay, PDeuel, LMacDonald, MHickey, CMuratori, LLouis, ELeserman, ADoucette, NUc, ERodnitzky, RVik, SDavis, RDietrich, SSegro, VErickson, DLucarelli, NBroyles, JDelarosa, JPanegyres, PSchmidt, ABarton, SSperin, EThiede, FZauber, SEWesson, MMcInnis, RWelsh, CColeman, A
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 180(3):232-245
Academic Journal
Layo-Carris DE; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Lubin EE; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.; Sangree AK; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.; Clark KJ; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.; Durham EL; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Gonzalez EM; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.; Smith S; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Angireddy R; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Wang XM; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Weiss E; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Mendoza-Londono R; Division of Clinical and Metabolic Genetics, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Dupuis L; Division of Clinical and Metabolic Genetics, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Damseh N; Division of Clinical and Metabolic Genetics, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Velasco D; Children's Nebraska, University of Nebraska Medical Center, Omaha, NE, USA.; Valenzuela I; Department of Clinical and Molecular Genetics and Rare Disease Unit Hospital Vall d'Hebron, Barcelona, Spain.; Medicine Genetics Group, Vall Hebron Research Institute, Barcelona, Spain.; Codina-Solà M; Department of Clinical and Molecular Genetics and Rare Disease Unit Hospital Vall d'Hebron, Barcelona, Spain.; Medicine Genetics Group, Vall Hebron Research Institute, Barcelona, Spain.; Ziats C; Shodair Children's Hospital, Helena, MT, USA.; Have J; Shodair Children's Hospital, Helena, MT, USA.; Clarkson K; Greenwood Genetic Center, Greenwood, SC, USA.; Steel D; UCL Great Ormond Street Institute of Child Health, London, UK.; Kurian M; UCL Great Ormond Street Institute of Child Health, London, UK.; Barwick K; UCL Great Ormond Street Institute of Child Health, London, UK.; Carrasco D; Department of Clinical Genetics, Cook Children's Hospital, Fort Worth, TX, USA.; Dagli AI; Orlando Health, Arnold Palmer Hospital For Children, Orlando, FL, USA.; Nowaczyk MJM; McMaster University Medical Centre, Hamilton, ON, Canada.; Hančárová M; Charles University Second Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.; Bendová Š; Charles University Second Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.; Prchalova D; Charles University Second Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.; Sedláček Z; Charles University Second Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.; Baxová A; Charles University First Faculty of Medicine and General University Hospital, Prague, Czech Republic.; Nowak CB; Division of Genetics and Metabolism, Massachusetts General Hospital for Children, Boston, MA, USA.; Douglas J; Harvard Medical School, Boston, MA, USA.; Chung WK; Harvard Medical School, Boston, MA, USA.; Boston Children's Hospital, Boston, MA, USA.; Longo N; University of Utah, Salt Lake City, UT, USA.; Platzer K; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Klöckner C; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Averdunk L; Institute of Human Genetics, Heinrich-Heine-University Düsseldorf, Medical Faculty, Düsseldorf, Germany.; Wieczorek D; Institute of Human Genetics, Heinrich-Heine-University Düsseldorf, Medical Faculty, Düsseldorf, Germany.; Krey I; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Zweier C; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054, Erlangen, Germany.; Department of Human Genetics, Inselspital Bern, University of Bern, Bern, Switzerland.; Reis A; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054, Erlangen, Germany.; Balci T; University of Western Ontario, London, ON, Canada.; Simon M; Department of Genetics, University Medical Center, Utrecht, Netherlands.; Kroes HY; Department of Genetics, University Medical Center, Utrecht, Netherlands.; Wiesener A; Department of Genetics, University Medical Center, Utrecht, Netherlands.; Vasileiou G; Department of Genetics, University Medical Center, Utrecht, Netherlands.; Marinakis NM; Laboratory of Medical Genetics, St. Sophia's Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece.; Veltra D; Laboratory of Medical Genetics, St. Sophia's Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece.; Sofocleous C; Laboratory of Medical Genetics, St. Sophia's Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece.; Kosma K; Laboratory of Medical Genetics, St. Sophia's Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece.; Traeger Synodinos J; Laboratory of Medical Genetics, St. Sophia's Children's Hospital, National and Kapodistrian University of Athens, Athens, Greece.; Voudris KA; Second Department of Paediatrics, University of Athens, 'P & A Kyriakou' Children's Hospital, Athens, Greece.; Vuillaume ML; Service de Génétique, CHU de Tours, Tours, France.; UMR1253, iBrain, Inserm, University of Tours, Tours, France.; Laboratoire de Biologie Médicale Multi-Sites SeqOIA, Paris, France.; Gueguen P; Service de Génétique, CHU de Tours, Tours, France.; UMR1253, iBrain, Inserm, University of Tours, Tours, France.; Laboratoire de Biologie Médicale Multi-Sites SeqOIA, Paris, France.; Derive N; Laboratoire de Biologie Médicale Multi-Sites SeqOIA, Paris, France.; Colin E; Service de Génétique Médicale, CHU d'Angers, Angers, France.; Battault C; Service de Génétique Médicale, CHU d'Angers, Angers, France.; Au B; University of Calgary, Calgary, AB, Canada.; Delatycki M; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville, VIC, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.; Wallis M; Tasmanian Clinical Genetics Service, Tasmanian Health Service, Hobart, TAS, Australia.; School of Medicine and Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.; Gallacher L; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville, VIC, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.; Majdoub F; Applied and Translational Neurogenomics Group, VIB Center for Molecular Neurology, Antwerp, Belgium.; Applied and Translational Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.; Medical Genetics Department, University Hedi Chaker Hospital of Sfax, Sfax, Tunisia.; Smal N; Applied and Translational Neurogenomics Group, VIB Center for Molecular Neurology, Antwerp, Belgium.; Applied and Translational Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.; Weckhuysen S; Applied and Translational Neurogenomics Group, VIB Center for Molecular Neurology, Antwerp, Belgium.; Applied and Translational Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.; Department of Pediatric Neurology, University Hospital Antwerp, Antwerp, Belgium.; Translational Neurosciences, Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium.; NEURO Research Centre of Excellence, University of Antwerp, Antwerp, Belgium.; Schoonjans AS; Department of Pediatric Neurology, University Hospital Antwerp, Antwerp, Belgium.; Department of Pediatrics, Duke University Hospital, Durham, NC, USA.; Kooy RF; Center of Medical Genetics, Antwerp University Hospital/University of Antwerp, Edegem, Belgium.; Meuwissen M; Department of Pediatrics, Duke University Hospital, Durham, NC, USA.; Center of Medical Genetics, Antwerp University Hospital/University of Antwerp, Edegem, Belgium.; Cocanougher BT; Department of Pediatrics, Duke University Hospital, Durham, NC, USA.; Taylor K; Division of Pediatric Neurology, Duke University Hospital, Durham, NC, USA.; Pizoli CE; Division of Pediatric Neurology, Duke University Hospital, Durham, NC, USA.; McDonald MT; Division of Medical Genetics, Duke University Hospital, Durham, NC, USA.; James P; DMG Children's Rehabilitative Services, Phoenix, AZ, USA.; Roeder ER; Department of Pediatrics, Baylor College of Medicine, San Antonio, TX, USA.; Littlejohn R; Department of Pediatrics, Baylor College of Medicine, San Antonio, TX, USA.; Borja NA; John T. Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL, USA.; Thorson W; John T. Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL, USA.; King K; Genetics Department, Mary Bridge Children's Hospital, Multicare Health System, Tacoma, WA, USA.; Stoeva R; Medical genetics department, Centre Hospitalier, Le Mans, France.; Suerink M; Department of Clinical Genetics, Leiden University Medical Center (LUMC), Leiden, The Netherlands.; Nibbeling E; Department of Clinical Genetics, Leiden University Medical Center (LUMC), Leiden, The Netherlands.; Baskin S; Department of Pediatrics, Baylor College of Medicine, San Antonio, TX, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; L E Guyader G; Service de Génétique médicale, Centre Labellisé Anomalies du Développement-Ouest Site, Poitiers, France.; Kaplan J; Nemours Children's Health, Wilmington, DE, USA.; Muss C; Nemours Children's Health, Wilmington, DE, USA.; Carere DA; GeneDx, Gaithersburg, MD, USA.; Bhoj EJK; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA. bhoje@chop.edu.; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. bhoje@chop.edu.; Bryant LM; Department of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA.
Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE
Academic Journal
Bergougnoux A; Génétique Moléculaire, CHU Montpellier, Montpellier, France; PhyMedExp, INSERM, CNRS UMR, Montpellier, France; Université de Montpellier, Montpellier, France.; Billet A; Laboratoire STIM, Université de Poitiers, Poitiers, France.; Ka C; Service de génétique moléculaire, CHRU Brest, Brest, France; Université de Brest, Inserm, UMR 1078, GGB, Brest, France.; Heller M; Service de Médecine Génomique des Maladies de Système et d'Organe, APHP Centre - Université de Paris, Hôpital Cochin, Paris, France.; Degrugillier F; Université Paris-Est Créteil, INSERM, IMRB, Créteil F-94010, France.; Vuillaume ML; Génétique Moléculaire, CHU Bordeaux, Bordeaux, France.; Thoreau V; Laboratoire NEUVACOD-3808, Université de Poitiers, Poitiers, France.; Sasorith S; Génétique Moléculaire, CHU Montpellier, Montpellier, France; PhyMedExp, INSERM, CNRS UMR, Montpellier, France.; Bareil C; Génétique Moléculaire, CHU Montpellier, Montpellier, France.; Thèze C; Génétique Moléculaire, CHU Montpellier, Montpellier, France.; Ferec C; Université de Brest, Inserm, UMR 1078, GGB, Brest, France.; Gac GL; Service de génétique moléculaire, CHRU Brest, Brest, France; Université de Brest, Inserm, UMR 1078, GGB, Brest, France.; Bienvenu T; Service de Médecine Génomique des Maladies de Système et d'Organe, APHP Centre - Université de Paris, Hôpital Cochin, Paris, France.; Bieth E; Génétique Médicale, CHU Toulouse, Toulouse, France.; Gaston V; Génétique Médicale, CHU Toulouse, Toulouse, France.; Lalau G; Biochimie et Biologie Moléculaire, CHU Lille, Lille, France.; Pagin A; Biochimie et Biologie Moléculaire, CHU Lille, Lille, France.; Malinge MC; Biochimie et Génétique, CHU Angers, Angers, France.; Dufernez F; Génétique, CHU Poitiers, Poitiers, France.; Lemonnier L; Association Vaincre la Mucoviscidose, Paris, France.; Koenig M; Génétique Moléculaire, CHU Montpellier, Montpellier, France; PhyMedExp, INSERM, CNRS UMR, Montpellier, France; Université de Montpellier, Montpellier, France.; Fergelot P; MRGM, INSERM UMR 1211 Université de Bordeaux, Bordeaux, France.; Claustres M; Université de Montpellier, Montpellier, France.; Taulan-Cadars M; PhyMedExp, INSERM, CNRS UMR, Montpellier, France; Université de Montpellier, Montpellier, France.; Kitzis A; Génétique, CHU Poitiers, Poitiers, France.; Reboul MP; Génétique Moléculaire, CHU Bordeaux, Bordeaux, France.; Becq F; Laboratoire STIM, Université de Poitiers, Poitiers, France.; Fanen P; AP-HP, Département de Biochimie-Biologie Moléculaire, Pharmacologie, Génétique Médicale, Hôpital Henri Mondor, Créteil F-94010, France.; Mekki C; AP-HP, Département de Biochimie-Biologie Moléculaire, Pharmacologie, Génétique Médicale, Hôpital Henri Mondor, Créteil F-94010, France.; Audrezet MP; Service de génétique moléculaire, CHRU Brest, Brest, France; Université de Brest, Inserm, UMR 1078, GGB, Brest, France.; Girodon E; Service de Médecine Génomique des Maladies de Système et d'Organe, APHP Centre - Université de Paris, Hôpital Cochin, Paris, France; INSERM U1151, Institut Necker Enfants Malades, Université de Paris, Paris, France.; Raynal C; Génétique Moléculaire, CHU Montpellier, Montpellier, France; PhyMedExp, INSERM, CNRS UMR, Montpellier, France. Electronic address: caroline.raynal@inserm.fr.
Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101128966 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-5010 (Electronic) Linking ISSN: 15691993 NLM ISO Abbreviation: J Cyst Fibros Subsets: MEDLINE
Huez C; Institute for Electronics Microelectronics and Nanotechnology (IEMN), CNRS, University of Lille, Av. Poincaré, Villeneuve d'Ascq, France. dominique.vuillaume@iemn.fr.; Guérin D; Institute for Electronics Microelectronics and Nanotechnology (IEMN), CNRS, University of Lille, Av. Poincaré, Villeneuve d'Ascq, France. dominique.vuillaume@iemn.fr.; Lenfant S; Institute for Electronics Microelectronics and Nanotechnology (IEMN), CNRS, University of Lille, Av. Poincaré, Villeneuve d'Ascq, France. dominique.vuillaume@iemn.fr.; Volatron F; Institut Parisien de Chimie Moléculaire (IPCM), CNRS, Sorbonne Université, 4 Place Jussieu, F-75005 Paris, France.; Calame M; EMPA, Transport at the Nanoscale Laboratory, 8600 Dübendorf, Switzerland.; Department of Physics and Swiss Nanoscience Institute, University of Basel, Klingelbergstrasse 82, 4056 Basel, Switzerland.; Perrin ML; EMPA, Transport at the Nanoscale Laboratory, 8600 Dübendorf, Switzerland.; Department of Information Technology and Electrical Engineering, ETH Zurich, 8092 Zurich, Switzerland.; Proust A; Institut Parisien de Chimie Moléculaire (IPCM), CNRS, Sorbonne Université, 4 Place Jussieu, F-75005 Paris, France.; Vuillaume D; Institute for Electronics Microelectronics and Nanotechnology (IEMN), CNRS, University of Lille, Av. Poincaré, Villeneuve d'Ascq, France. dominique.vuillaume@iemn.fr.
Publisher: RSC Pub Country of Publication: England NLM ID: 101525249 Publication Model: Electronic Cited Medium: Internet ISSN: 2040-3372 (Electronic) Linking ISSN: 20403364 NLM ISO Abbreviation: Nanoscale Subsets: PubMed not MEDLINE; MEDLINE
Academic Journal
Huez C; Institute for Electronics Microelectronics and Nanotechnology (IEMN), CNRS, University of Lille, Av. Poincaré, Villeneuve d'Ascq, France. dominique.vuillaume@iemn.fr.; Guérin D; Institute for Electronics Microelectronics and Nanotechnology (IEMN), CNRS, University of Lille, Av. Poincaré, Villeneuve d'Ascq, France. dominique.vuillaume@iemn.fr.; Lenfant S; Institute for Electronics Microelectronics and Nanotechnology (IEMN), CNRS, University of Lille, Av. Poincaré, Villeneuve d'Ascq, France. dominique.vuillaume@iemn.fr.; Volatron F; Institut Parisien de Chimie Moléculaire (IPCM), CNRS, Sorbonne Université, 4 Place Jussieu, F-75005 Paris, France.; Calame M; EMPA, Transport at the Nanoscale Laboratory, 8600 Dübendorf, Switzerland.; Dept. of Physics and Swiss Nanoscience Institute, University of Basel, Klingelbergstrasse 82, 4056 Basel, Switzerland.; Perrin ML; EMPA, Transport at the Nanoscale Laboratory, 8600 Dübendorf, Switzerland.; Department of Information Technology and Electrical Engineering, ETH Zurich, 8092 Zurich, Switzerland.; Proust A; Institut Parisien de Chimie Moléculaire (IPCM), CNRS, Sorbonne Université, 4 Place Jussieu, F-75005 Paris, France.; Vuillaume D; Institute for Electronics Microelectronics and Nanotechnology (IEMN), CNRS, University of Lille, Av. Poincaré, Villeneuve d'Ascq, France. dominique.vuillaume@iemn.fr.
Publisher: RSC Pub Country of Publication: England NLM ID: 101525249 Publication Model: Electronic Cited Medium: Internet ISSN: 2040-3372 (Electronic) Linking ISSN: 20403364 NLM ISO Abbreviation: Nanoscale Subsets: PubMed not MEDLINE; MEDLINE
Academic Journal
Cordovado A; UMR 1253, iBrain, University of Tours, INSERM, Tours 37032, France.; Schaettin M; Department of Molecular Life Sciences, Neuroscience Center Zurich, University of Zurich, Zurich 8057, Switzerland.; Jeanne M; UMR 1253, iBrain, University of Tours, INSERM, Tours 37032, France.; Genetics Department, University Hospital of Tours, Tours 37044, France.; Panasenkava V; UMR 1253, iBrain, University of Tours, INSERM, Tours 37032, France.; Denommé-Pichon AS; Functional Unit in Innovative Genomic Diagnosis of Rare Diseases, FHU-TRANSLAD, Dijon-Bourgogne University Hospital, Dijon 21079, France.; UMR1231 GAD, INSERM - Bourgogne-Franche Comté University, Dijon 21000, France.; Keren B; Genetics Department, Pitié-Salpêtrière Hospital, AP-HP. Sorbonne University, Paris 75651, France.; Mignot C; Genetics Department, Pitié-Salpêtrière Hospital, AP-HP. Sorbonne University, Paris 75651, France.; Doco-Fenzy M; University Hospital Reims, AMH2, Genetics Division, SFR CAP santé EA3801, Reims 51100, France.; Rodan L; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Boston, MA 02115, USA.; Department of Neurology, Boston Children's Hospital, Boston, MA 02115, USA.; Ramsey K; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, AZ 85012, USA.; Narayanan V; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, AZ 85012, USA.; Jones JR; Molecular Diagnostic Laboratory, Greenwood Genetic Center, Greenwood, SC 29646, USA.; Prijoles EJ; Greenwood Genetic Center, Greenwood, SC 29646, USA.; Mitchell WG; Neurology Division, Keck School of Medicine, University of Southern California, Children's Hospital Los Angeles, CA 90027, USA.; Ozmore JR; Dartmouth Hitchcock Medical Center, Lebanon, NH 03766, USA.; Juliette K; Neurology Department, Gillette Children's Specialty Healthcare, St Paul, MN 55101, USA.; Torti E; GeneDx, Gaithersburg, MD 20877, USA.; Normand EA; GeneDx, Gaithersburg, MD 20877, USA.; Granger L; Genetics Division, Department of Pediatric Development and Rehabilitation, Randall Children's Hospital, Portland, OR 97227, USA.; Petersen AK; Genetics Division, Department of Pediatric Development and Rehabilitation, Randall Children's Hospital, Portland, OR 97227, USA.; Au MG; Department of Genetics and Metabolism, University of Kentucky, Lexington, KY 40536, USA.; Matheny JP; Department of Genetics and Metabolism, University of Kentucky, Lexington, KY 40536, USA.; Phornphutkul C; Division of Human Genetics, Department of Pediatrics, Warren Alpert Medical School of Brown University, Hasbro Children's Hospital, Providence, RI 02903, USA.; Chambers MK; Division of Genetics, Rhode Island Hospital, Hasbro Children's Hospital, Providence, RI 02903, USA.; Fernández-Ramos JA; Pediatric Neurology Unit, Department of Pediatrics, University Hospital Reina Sofía, IMIBIC and CIBERER, Córdoba 14004, Spain.; López-Laso E; Pediatric Neurology Unit, Department of Pediatrics, University Hospital Reina Sofía, IMIBIC and CIBERER, Córdoba 14004, Spain.; Kruer MC; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ 85016, USA.; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ 85004, USA.; Bakhtiari S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ 85016, USA.; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ 85004, USA.; Zollino M; Università Cattolica Sacro Cuore, Dipartimento Scienze della Vita e Sanità Pubblica, Sezione di Medicina Genomica, Roma 00168, Italy.; Fondazione Policlinico A. Gemelli IRCCS, U. O. C. Genetica Medica, Roma 00168, Italy.; Morleo M; Telethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Naples 80078, Italy.; Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples 80138, Italy.; Marangi G; Università Cattolica Sacro Cuore, Dipartimento Scienze della Vita e Sanità Pubblica, Sezione di Medicina Genomica, Roma 00168, Italy.; Fondazione Policlinico A. Gemelli IRCCS, U. O. C. Genetica Medica, Roma 00168, Italy.; Mei D; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Meyer Children's Hospital, Member of ERN Epicare, University of Florence, Florence 50139, Italy.; Pisano T; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Meyer Children's Hospital, Member of ERN Epicare, University of Florence, Florence 50139, Italy.; Guerrini R; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Meyer Children's Hospital, Member of ERN Epicare, University of Florence, Florence 50139, Italy.; Louie RJ; Molecular Diagnostic Laboratory, Greenwood Genetic Center, Greenwood, SC 29646, USA.; Childers A; Molecular Diagnostic Laboratory, Greenwood Genetic Center, Greenwood, SC 29646, USA.; Everman DB; Molecular Diagnostic Laboratory, Greenwood Genetic Center, Greenwood, SC 29646, USA.; Isidor B; Medical Genetics Service, Clinical Genetics Unit, University Hospital of Nantes, Hôtel Dieu, Nantes 44093, France.; Audebert-Bellanger S; Clinical Genetics Service, University Hospital of Brest, Morvan Hospital, Brest 29609, France.; Odent S; Clinical Genetics Service, University Hospital, Genetic and Development Institute of Rennes IGDR, UMR 6290 University of Rennes, ITHACA ERN, Rennes 35203, France.; Bonneau D; Department of Medical Genetics, University Hospital of Angers and Mitovasc INSERM 1083, CNRS 6015, Angers 49000, France.; Gilbert-Dussardier B; Medical Genetics, University Hospital, La Milétrie, BP 577, Poitiers 86021, France.; Redon R; INSERM, CNRS, UNIV Nantes, Thorax Institute, Nantes 44007, France.; Bézieau S; INSERM, CNRS, UNIV Nantes, Thorax Institute, Nantes 44007, France.; Medical Genetics Service, University Hospital of Nantes, Nantes 44093, France.; Laumonnier F; UMR 1253, iBrain, University of Tours, INSERM, Tours 37032, France.; Stoeckli ET; Department of Molecular Life Sciences, Neuroscience Center Zurich, University of Zurich, Zurich 8057, Switzerland.; Toutain A; UMR 1253, iBrain, University of Tours, INSERM, Tours 37032, France.; Genetics Department, University Hospital of Tours, Tours 37044, France.; Vuillaume ML; UMR 1253, iBrain, University of Tours, INSERM, Tours 37032, France.; Genetics Department, University Hospital of Tours, Tours 37044, France.
Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Academic Journal
Halewa J; UMR1253, iBrain, INSERM, University of Tours, Tours, France.; Marouillat S; UMR1253, iBrain, INSERM, University of Tours, Tours, France.; Dixneuf M; UMR1253, iBrain, INSERM, University of Tours, Tours, France.; Thépault RA; UMR1253, iBrain, INSERM, University of Tours, Tours, France.; Ung DC; UMR1253, iBrain, INSERM, University of Tours, Tours, France.; Chatron N; Department of Genetics, Hospices Civils de Lyon, Lyon, France.; Institut NeuroMyoGène, CNRS UMR-5310, INSERM U-1217, Univ Lyon, Université Claude Bernard Lyon 1, Lyon, France.; Gérard B; Laboratoire de diagnostic génétique, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Ghoumid J; EA7364 RADEME, Clinique de Génétique Guy Fontaine, Université de Lille, CHU de Lille, Lille, France.; Lesca G; Department of Genetics, Hospices Civils de Lyon, Lyon, France.; Institut NeuroMyoGène, CNRS UMR-5310, INSERM U-1217, Univ Lyon, Université Claude Bernard Lyon 1, Lyon, France.; Till M; Department of Genetics, Hospices Civils de Lyon, Lyon, France.; Smol T; EA7364 RADEME, Institut de Génétique Médicale, Université de Lille, CHU de Lille, Lille, France.; Couque N; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.; Ruaud L; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.; INSERM, UMR1141, Denis Diderot School of Medicine, Paris University, Paris, France.; Chune V; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.; Grotto S; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.; INSERM, UMR1141, Denis Diderot School of Medicine, Paris University, Paris, France.; Verloes A; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.; INSERM, UMR1141, Denis Diderot School of Medicine, Paris University, Paris, France.; Vuillaume ML; UMR1253, iBrain, INSERM, University of Tours, Tours, France.; Service de Génétique, Centre hospitalier régional universitaire de Tours, Tours, France.; Toutain A; UMR1253, iBrain, INSERM, University of Tours, Tours, France.; Service de Génétique, Centre hospitalier régional universitaire de Tours, Tours, France.; Raynaud M; UMR1253, iBrain, INSERM, University of Tours, Tours, France.; Service de Génétique, Centre hospitalier régional universitaire de Tours, Tours, France.; Laumonnier F; UMR1253, iBrain, INSERM, University of Tours, Tours, France.; Service de Génétique, Centre hospitalier régional universitaire de Tours, Tours, France.
Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Academic Journal
Jeanne M; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.; Vuillaume ML; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.; Ung DC; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.; Vancollie VE; Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, Hinxton, UK.; Wagner C; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France.; Collins SC; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France.; Vonwill S; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; Haye D; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; Chelloug N; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; Pfundt R; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands.; Kummeling J; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands.; Moizard MP; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; Marouillat S; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.; Kleefstra T; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands.; Yalcin B; Centre National de la Recherche Scientifique, UMR 7104, Illkirch, France.; Institut National de la Santé et de la Recherche Médicale (Inserm), U 1258, Illkirch, France.; Université de Strasbourg, Illkirch, France.; Laumonnier F; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France. frederic.laumonnier@inserm.fr.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France. frederic.laumonnier@inserm.fr.; Toutain A; Service de Génétique, Centre Hospitalier Régional Universitaire, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.
Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE
Academic Journal
Abdelfattah F; Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.; Kariminejad A; Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran.; Kahlert AK; Institut für Klinische Genetik, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.; Department of Congenital Heart Disease and Pediatric Cardiology, University Hospital Schleswig-Holstein, Kiel, Germany.; Morrison PJ; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, UK.; Gumus E; Division of Medical Genetics, School of Medicine, Harran University, Sanliurfa, Turkey.; Mathews KD; Carver College of Medicine, University of Iowa, Iowa City, Iowa.; Darbro BW; Carver College of Medicine, University of Iowa, Iowa City, Iowa.; Amor DJ; Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, The University of Melbourne, Melbourne, Victoria, Australia.; Royal Children's Hospital, Parkville, Victoria, Australia.; Walsh M; Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Sznajer Y; Centre de Génétique Humaine, Cliniques Universitaires Saint Luc, Université Catholique de Louvain, Brussels, Belgium.; Weiß L; Institut für Klinische Genetik, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.; Weidensee S; Human Medical Genetics, Erfurt, Germany.; Chitayat D; Department of Obstetrics and Gynecology, The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.; Division of Clinical and Metabolic Genetics, The Hospital for SickKids, University of Toronto, Toronto, Ontario, Canada.; Shannon P; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.; Bermejo-Sánchez E; ECEMC (Spanish Collaborative Study of Congenital Malformations), Research Unit on Congenital Anomalies (UIAC), Institute of Rare Diseases Research (IIER), Institute of Health Carlos III, Ministry of Science and Innovation, Madrid, Spain.; Riaño-Galán I; AGC de Pediatría, Hospital Universitario Central de Asturias, Oviedo, Spain.; IUOPA-Departamento de Medicina-ISPA, Universidad de Oviedo, Oviedo, Spain.; CIBER de Epidemiologia y Salud Pública, Madrid, Spain.; Hayes I; Genetic Health Service New Zealand, Auckland Hospital, Auckland, New Zealand.; Poke G; Genetic Health Service New Zealand, Wellington Regional Hospital, Wellington, New Zealand.; Rooryck C; MRGM INSERM U1211, CHU de Bordeaux, Service de Génétique Médicale, University of Bordeaux, Bordeaux, France.; Pennamen P; MRGM INSERM U1211, CHU de Bordeaux, Service de Génétique Médicale, University of Bordeaux, Bordeaux, France.; Khung-Savatovsky S; Unité de Fœtopathologie, Hôpital Universitaire Robert-Debré, Paris, France.; Toutain A; Service de Génétique, CHU de Tours, UMR 1253, iBrain, Université de Tours, INSERM, Tours, France.; Vuillaume ML; Service de Génétique, CHU de Tours, UMR 1253, iBrain, Université de Tours, INSERM, Tours, France.; Ghaderi-Sohi S; Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran.; Kariminejad MH; Kariminejad-Najmabadi Pathology and Genetics Center, Tehran, Iran.; Weinert S; Department of Cardiology and Angiology, Internal Medicine, University Hospital Magdeburg, Magdeburg, Germany.; Sticht H; Institute of Biochemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Zenker M; Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.; Schanze D; Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.
Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
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