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One or more keywords matched the following items that are connected to Gilliam, T. Conrad
Item TypeName
Concept Fragile X Syndrome
Concept Memory, Short-Term
Concept Syndrome
Concept Asperger Syndrome
Concept Menkes Kinky Hair Syndrome
Academic Article Catechol-O-methyltransferase (COMT) genotypes and working memory: associations with differing cognitive operations.
Academic Article Strong association of de novo copy number mutations with autism.
Academic Article Rapid selection response for contextual fear conditioning in a cross between C57BL/6J and A/J: behavioral, QTL and gene expression analysis.
Academic Article A genomewide screen for autism susceptibility loci.
Academic Article LGI1 mutations in autosomal dominant partial epilepsy with auditory features.
Academic Article Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.
Academic Article Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome.
Academic Article An international symposium on Wilson's and Menkes' diseases.
Academic Article A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene.
Academic Article DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory ability.
Academic Article Genetic disorders of copper metabolism.
Academic Article A genetic linkage map of the chromosome 4 short arm.
Academic Article Heterologous expression of the metal-binding domains of human copper-transporting ATPases (P1-ATPases).
Academic Article Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28.
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