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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
Homozygote
Academic Article
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.
Academic Article
Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3.
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
Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy.
Academic Article
Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.
Academic Article
Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice.
Search Criteria
Homozygote