D038062DisordersC05.660.585.988C16.131.621.585.988450.995394Upper Extremity Deformities, Congenitalprns:emailEncryptedemail addressprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:mainImagephotoprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:meshTreeNumberMeSH tree numberprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:positionInDepartmentposition in departmentprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierDepartmentvivo:hrJobTitleHR job titleInformation ResourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson22543974Smemo S, Campos LC, Moskowitz IP, Krieger JE, Pereira AC, Nobrega MAHuman molecular geneticsRegulatory variation in a TBX5 enhancer leads to isolated congenital heart disease. Hum Mol Genet. 2012 Jul 15; 21(14):3255-63.Hum Mol Genet2012-04-27T00:00:002012Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.0.4356610.1089154research area of0.4896240.1486613subject area forHuman GeneticsUniversity of ChicagoEdenHaverfieldEden Haverfield41.78927490000000-87.601250000000001297Haverfield, EdenScottSmemoScott Smemo41.78927490000000-87.601250000000001332Smemo, ScottPostdoctoral FellowMarcelo A.Nobrega2W1rGaQSGMzMknJtY0fp/Cv/+94=Marcelo A. Nobrega41.78927490000000-87.601250000000002531Nobrega, Marcelo A.ProfessorIvanMoskowitz3m9mGKoaDuXNi1pxY07n8GT98IW47aA=Ivan Moskowitz41.78927490000000-87.6012500000000037Moskowitz, IvanProfessortrue1true1ProfessorProfessortrue1Postdoctoral FellowPostdoctoral Fellowtrue1ProfessorProfessor24218399Dempsey MA, Knight Johnson AE, Swope BS, Moldenhauer JS, Sroka H, Chong K, Chitayat D, Briere L, Lyon H, Palmer N, Gopalani S, Siebert JR, Lévesque S, Leblanc J, Menzies D, Haverfield E, Das SPrenatal diagnosisMolecular confirmation of nine cases of Cornelia de Lange syndrome diagnosed prenatally. Prenat Diagn. 2014 Feb; 34(2):163-7.Prenat Diagn2013-12-09T00:00:002013Molecular confirmation of nine cases of Cornelia de Lange syndrome diagnosed prenatally.Pediatrics-Cardiology28057264Steimle JD, Moskowitz IPCurrent topics in developmental biologyTBX5: A Key Regulator of Heart Development. Curr Top Dev Biol. 2017; 122:195-221.Curr Top Dev Biol2016-09-28T00:00:002016TBX5: A Key Regulator of Heart Development.