Browsing by Author Marshall, CR

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TitleAuthor(s)Issue Date
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS)
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012
2012
 
Pinto, DPagnamenta, ATKlei, LAnney, RMerico, DRegan, RConroy, JMagalhaes, TRCorreia, CAbrahams, BSAlmeida, JBacchelli, EBader, GDBailey, AJBaird, GBattaglia, ABerney, TBolshakova, NBölte, SBolton, PFBourgeron, TBrennan, SBrian, JBryson, SECarson, ARCasallo, GCasey, JChung, BHYCochrane, LCorsello, CCrawford, ELCrossett, ACytrynbaum, CDawson, GDe Jonge, MDelorme, RDrmic, IDuketis, EDuque, FEstes, AFarrar, PFernandez, BAFolstein, SEFombonne, EFreitag, CMGilbert, JGillberg, CGlessner, JTGoldberg, JGreen, AGreen, JGuter, SJHakonarson, HHeron, EAHill, MHolt, RHowe, JLHughes, GHus, VIgliozzi, RKim, CKlauck, SMKolevzon, AKorvatska, OKustanovich, VLajonchere, CMLamb, JALaskawiec, MLeboyer, MLe Couteur, ALeventhal, BLLionel, ACLiu, XQLord, CLotspeich, LLund, SCMaestrini, EMahoney, WMantoulan, CMarshall, CRMcconachie, HMcdougle, CJMcgrath, JMcmahon, WMMerikangas, AMigita, OMinshew, NJMirza, GKMunson, JNelson, SFNoakes, CNoor, ANygren, GOliveira, GPapanikolaou, KParr, JRParrini, BPaton, TPickles, APilorge, MPiven, JPonting, CPPosey, DJPoustka, APoustka, FPrasad, ARagoussis, JRenshaw, KRickaby, JRoberts, WRoeder, KRoge, BRutter, MLBierut, LJRice, JPSalt, JSansom, KSato, DSegurado, RSequeira, AFSenman, LShah, NSheffield, VCSoorya, LSousa, IStein, OSykes, NStoppioni, VStrawbridge, CTancredi, RTansey, KThiruvahindrapduram, BThompson, APThomson, STryfon, ATsiantis, JVan Engeland, HVincent, JBVolkmar, FWallace, SWang, KWang, ZWassink, THWebber, CWeksberg, RWing, KWittemeyer, KWood, SWu, JYaspan, BLZurawiecki, DZwaigenbaum, LBuxbaum, JDCantor, RMCook, EHCoon, HCuccaro, MLDevlin, BEnnis, SGallagher, LGeschwind, DHGill, MHaines, JLHallmayer, JMiller, JMonaco, APNurnberger Jr, JIPaterson, ADPericakVance, MASchellenberg, GDSzatmari, PVicente, AMVieland, VJWijsman, EMScherer, SWSutcliffe, JSBetancur, C
2010
 
2012
Genome-wide copy number analysis uncovers a new HSCR gene: NRG3
Proceeding/Conference:International Congress of Human Genetics, ICHG 2011
2011
 
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