19161147Rajab A, Aldinger KA, El-Shirbini HA, Dobyns WB, Ross MEAmerican journal of medical genetics. Part ABrain Diseases; Calcinosis; Chromosomes, Human, Pair 2; Developmental Disabilities; MicrocephalyAdolescent; Adult; Basal Ganglia; Body Size; Cerebral Cortex; Child; Child, Preschool; Chromosome Mapping; Diagnostic Imaging; Family Health; Female; Humans; Lod Score; Male; Oman; SyndromeRecessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2. Am J Med Genet A. 2009 Feb; 149A(2):129-37.Am J Med Genet A2009-02-01T00:00:002009Recessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2.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 nameOrganizationPersonD000293Living Beings111389680.40057AdolescentD001927Disorders951800.889777Brain DiseasesD000328Living Beings1578255770.254454AdultD002540Anatomy1535840.720264Cerebral CortexD002889Anatomy35850.976047Chromosomes, Human, Pair 2D001479Anatomy30420.973127Basal GangliaD002114Disorders932240.872819CalcinosisD002648Living Beings93969130.440068ChildD002658Disorders631940.865831Developmental DisabilitiesD002874Procedures22910740.772788Chromosome MappingD002675Living Beings65236080.594978Child, PreschoolD003952Procedures2064680.722063Diagnostic ImagingD008831Disorders19750.955455MicrocephalyD005260Physiology1992444050.191184FemaleD006801Living Beings2262862810.130064HumansD013577Disorders2074460.911443SyndromeWilliamDobynsWilliam B. Dobyns0.000000000000000.000000000000002964Dobyns, WilliamPROFESSOR D008297Physiology1931408600.201635MaleD009850Geographic Areas350.99883OmanD049628Concepts & IdeasPhysiology53910.942077Body SizeD005192Concepts & Ideas921620.947031Family HealthD008126Concepts & Ideas401520.977031Lod ScoreHuman GeneticsUniversity of Chicagotrue1PROFESSOR PROFESSOR Authorship 6632440.08744980.08744981authors10.2521has subject area