First Header Logo Second Header Logo

Search Result Details

Back to Search Results
This page shows the details of why an item matched the keywords from your search.
Search Results
Snively, Beverly
One or more keywords matched the following items that are connected to Snively, Beverly
Item TypeName
Academic Article Hemochromatosis and iron-overload screening in a racially diverse population.
Academic Article Mixture models of serum iron measures in population screening for hemochromatosis and iron overload.
Academic Article Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening.
Academic Article Screening for iron overload: lessons from the hemochromatosis and iron overload screening (HEIRS) study.
Academic Article Geographic and racial/ethnic differences in HFE mutation frequencies in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.
Academic Article Hemochromatosis (HFE) gene splice site mutation IVS5+1 G/A in North American Vietnamese with and without phenotypic evidence of iron overload.
Academic Article Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study.
Academic Article ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.
Concept Mutation
Concept Point Mutation
Concept Mutation, Missense
Academic Article Cognitive impairment in rapid-onset dystonia-parkinsonism.
Academic Article ATP1A3 Mutation in Adult Rapid-Onset Ataxia.
Academic Article Revising rapid-onset dystonia-parkinsonism: Broadening indications for ATP1A3 testing.
Academic Article Auditory-perceptual voice and speech evaluation in ATP1A3 positive patients.
Grant Clinical, Genetic, And Cellular Consequences of Mutations in Na,K-ATPase ATP1A3
Search Criteria
  • Mutation