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Gilliam, T. Conrad
One or more keywords matched the following items that are connected to
Gilliam, T. Conrad
Item Type
Name
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.
Search Criteria
Short
QT
syndrome