7904586Brzustowicz LM, Mérette C, Kleyn PW, Lehner T, Castilla LH, Penchaszadeh GK, Das K, Munsat TL, Ott J, Gilliam TCHuman heredityChromosomes, Human, Pair 5; Muscular Atrophy, SpinalAdolescent; Alleles; Child; Child, Preschool; Chromosome Mapping; Chronic Disease; DNA, Satellite; Female; Genetic Linkage; Genetic Variation; Genotype; Humans; Lod Score; Male; Odds Ratio; Pedigree; Polymorphism, Restriction Fragment Length; Retrospective StudiesAssessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy. Hum Hered. 1993 Nov-Dec; 43(6):380-7.Hum Hered1993-11-01T00:00:001993Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.prns:emailEncryptedemail addressprns: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:mainImagephotoprns: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 Beings111389680.40057AdolescentD000483Genes & Molecular Sequences29311270.757225AllelesD002648Living Beings93969130.440068ChildD002874Procedures22910740.772788Chromosome MappingD002895Anatomy361080.956987Chromosomes, Human, Pair 5D002675Living Beings65236080.594978Child, PreschoolD002908DisordersLiving Beings3839680.756988Chronic DiseaseD004276Chemicals & Drugs6180.995435DNA, SatelliteD009134Disorders9240.986133Muscular Atrophy, SpinalD010375Concepts & Ideas1929660.83743PedigreeD005260Physiology1992444050.191184FemaleD012150Physiology551470.972413Polymorphism, Restriction Fragment LengthD006801Living Beings2262862810.130064HumansAuthorship 98809D014644Phenomena29413490.59631Genetic VariationD008297Physiology1931408600.201635Male0.03038160.03038161authors10.2520has subject areaD016017Concepts & Ideas2896770.843127Odds RatioD005838Physiology41118500.686761GenotypeD008040Concepts & IdeasPhysiology1206230.858672Genetic LinkageD008126Concepts & Ideas401520.977031Lod ScoreD012189Concepts & Ideas114884310.376547Retrospective StudiesHuman GeneticsUniversity of ChicagoT. ConradGilliam0GtlB6gUFL35hHlsaUXv9Gq0+s+oT. Conrad Gilliam41.78927490000000-87.60125000000000109Gilliam, T. ConradProfessortrue1ProfessorProfessor