Browsing by Author Miao, X

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TitleAuthor(s)Issue DateViews
 
2011
117
 
2013
120
 
2008
119
 
Evaluation of thyroid transcription factor 1 (TTF-1) as a Hirschsprung's disease (HSCR) locus by mutation analysis
Proceeding/Conference:Annual Meeting of the Pacific Association of Pediatric Surgeons, PAPS 2006
2006
113
 
2005
105
 
2012
201
 
2013
114
 
2010
156
 
Higher prevalence of Hirschsprung disease in China explained by a common RET mutation
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2006
2006
88
 
2008
129
 
2007
92
 
2007
126
 
Wang, ZZhu, BZhang, MParikh, HJia, JChung, CCSampson, JNHoskins, JWHutchinson, ABurdette, LIbrahim, AHsing, AWHsiung, CAHu, NAdjei, AAGross, MRuder, AMHu, WHu, ZHuang, MSWang, CCanzian, FLim, WYHunter, DJSimon, MInskip, PDMa, JIto, HJacobs, EJRyu, JSJacobs, KBYang, HPCao, GKim, YCJenab, MJi, BTKoh, WPAhlbom, AJohansen, CJohansson, MSouthey, MCJohnson, ASanson, MCaporaso, NEKaaks, RPrescott, JGastier-Foster, JMKamat, AMYang, PCKamineni, AKohno, TMalats, NKolonel, LNKooperberg, CCarrato, AKratz, CPYu, CJAldrich, MKrogh, VKunitoh, HStampfer, MCortessis, VKKurtz, RCShen, HKurucu, NArslan, AALan, QAmbrosone, CBLathrop, MWang, JSchned, AMannisto, SMarina, NMastrangelo, GMatsuo, KCrawford, EDKitahara, CMMcGlynn, KAAustin, MABerndt, SIMcKean-Cowdin, RGorlick, RMcNeill, LHGillanders, EMMcWilliams, RRGaziano, JMMelin, BSCarreon, TAmos, CMeltzer, PSCussenot, OMensah, JEMiao, XWang, SSMichaud, DSYe, YKhanna, CStattin, PCarta, AMondul, AMMoore, LEMuir, KNiwa, SGerhard, DSLissowska, JBeane Freeman, LEOlson, SHOrr, NAndersson, UChang, GCSierri, SPanico, SYeboah, EDPark, JYStern, MCPatel, AVPatino-Garcia, AWeiderpass, EPavanello, SDavis, FGRisch, HAPeeters, PHPeplonska, BSchumacher, FRGiffen, CAPeters, UPetersen, GMYin, ZPicci, PWeinstein, SJAndriole, GVan Den Eeden, SKLecanda, FPike, MCDe Vivo, IPorru, SSchwartz, AGStevens, VLSchwartz, KLSchwenn, MScotlandi, KDuell, EJGoggins, MArici, CSeow, AYu, KKhaw, KTSerra, CWu, XSerra, MSesso, HDGiovannucci, ELSeveri, GChang, ISWentzensen, NStolzenberg-Solomon, RZStram, DOStrom, SSSu, WCKim, CSund, MGrossman, HBHallmans, GSung, SWLindstrom, SSwerdlow, ALi, DBaris, DLee, KMTan, WHautman, CTanaka, HAlbanes, DTang, WTang, ZZChang-Claude, JTardon, ADing, TPu, XYuan, JMTay, ETaylor, PRTettey, YThomas, DMLee, MPSpector, LHaiman, CATirabosco, RBarkauskas, DAGoldstein, AMYatabe, YTjonneland, ADinney, CPTobias, GSZanetti, KAToro, JRTravis, RCChe, XTrichopoulos, DKim, ISTroisi, RTruelove, AWheeler, WLe Marchand, LTsai, YHTucker, MADi Stefano, ALTumino, RChen, CJGonzalez, CShen, MBassig, BAKim, YHVan Den Berg, DWhite, EZeleniuch-Jacquotte, AWiencke, JKWolk, AWolpin, BMKlein, APGreene, MHWong, MPElena, JWPurdue, MPWrensch, MConti, DBerg, CDWu, CLiao, LMWu, TChen, CYZheng, WBertazzi, PAZhou, BMirabello, LQiao, YLSavage, SALiu, JAmiano, PKraft, PChanock, SJSiddiq, AGrubb, RShete, SYeager, MGarcia-Closas, RLandi, MTGiles, GGShi, JChatterjee, NAmundadottir, LTKim, YTVermeulen, RFan, JHBiritwum, RBBlack, ABlot, WBoeing, HShiraishi, KYing, CBoffetta, PGu, JLin, DDeng, XBolton, KKang, CHBoutron-Ruault, MCFeigelson, HSBracci, PMBrennan, PBrinton, LARajaraman, PBrotzman, MBueno-de-Mesquita, HBChen, CHShu, XOBuring, JEButler, MAJung, YJCai, QLin, JWu, YLGuan, PRiboli, ECancel-Tassin, GChen, CFeychting, MChen, KYChen, YMChokkalingam, APLinet, MSChu, LWKlein, RVineis, PClavel-Chapelon, FKaragas, MRaj, PSColditz, GASierrasesumaga, LColt, JSFigueroa, JDHankinson, SEFlanagan, AMFraumeni, JFVisvanathan, KFreedman, NDSpitz, MGokgoz, NFridley, BLFuchs, CSLjungberg, BWunder, JSGago-Dominguez, MLau, CCGallinger, SLerner, SPGao, YTGapstur, SMGarcia-Closas, MRodabough, RJKogevinas, MHarris, CCHartge, PHattinger, CHayes, RBXiang, YBDiver, WRHe, QLloreta, JSihoe, ADLHelman, LAndrulis, ILHenderson, BEAllen, NEHenriksson, RAbnet, CCHoffman-Bolton, JVogel, UHohensee, CHolly, EAXu, JHong, YCHoover, RNRothman, NHosgood, HDSilverman, DTCook, MBLu, DWang, CHsiao, CF
2014
114
 
2007
153
 
2010
133
2006
107
 
2006
123
 
MNX1 (HLXB9) mutations in Currarino patients
Journal:Journal of Pediatric Surgery
2009
163
 
Mutational analysis of SHH and GLI3 in anorectal malformations
Journal:Birth Defects Research Part A - Clinical and Molecular Teratology
2008
196
 
2011
232