20571508Carr CW, Moreno-De-Luca D, Parker C, Zimmerman HH, Ledbetter N, Martin CL, Dobyns WB, Abdul-Rahman OAEuropean journal of human genetics : EJHGAbnormalities, Multiple; Arnold-Chiari Malformation; Developmental Disabilities; Forkhead Transcription Factors; Haploinsufficiency; Repressor ProteinsChild, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 3; Comparative Genomic Hybridization; Epilepsy; Humans; Infant; Language Development Disorders; MaleChiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency. Eur J Hum Genet. 2010 Nov; 18(11):1216-20.Eur J Hum Genet2010-06-23T00:00:002010Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency.prns:fullNamefull nameprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:hasSubjectAreaMajorTopicListhas major subject area listprns:hasSubjectAreaMinorTopicListhas minor subject area listprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns: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 Identifiervivo:authorRankauthor rank in publicationAuthorshipDepartmentvivo:hasSubjectAreahas subject areavivo:hrJobTitleHR job titleInformation Resourcevivo:informationResourceInAuthorshipauthorsvivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonD000015Disorders842320.867856Abnormalities, MultipleD001139Disorders17430.939295Arnold-Chiari MalformationD002893Anatomy29540.981072Chromosomes, Human, Pair 3D002658Disorders631940.865831Developmental DisabilitiesD002872Disorders872280.920654Chromosome DeletionD004827Disorders803950.728734EpilepsyD002675Living Beings65236080.594978Child, PreschoolD007223Living Beings60430360.613076InfantD007805Disorders16240.978469Language Development DisordersD012097Chemicals & Drugs1894030.777372Repressor ProteinsD006801Living Beings2262862810.130064HumansWilliamDobynsWilliam B. Dobyns0.000000000000000.000000000000002964Dobyns, WilliamPROFESSOR D008297Physiology1931408600.201635MaleD057895Concepts & IdeasDisorders39620.944362HaploinsufficiencyD051858Chemicals & Drugs1021660.90291Forkhead Transcription FactorsD055028Procedures27390.984812Comparative Genomic HybridizationHuman GeneticsUniversity of Chicagotrue1PROFESSOR PROFESSOR Authorship 7229670.09628190.09628191authors10.2515has subject area