The University of Chicago 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
Gilliam, T. Conrad
One or more keywords matched the following items that are connected to Gilliam, T. Conrad
Item TypeName
Concept Muscular Atrophy, Spinal
Academic Article High resolution physical map of the region surrounding the spinal muscular atrophy gene.
Academic Article Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.
Academic Article Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene.
Academic Article Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy.
Academic Article Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B.
Academic Article An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy.
Academic Article A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions.
Academic Article Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues.
Academic Article Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13.
Academic Article Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophy.
Academic Article Differential SMN2 expression associated with SMA severity.
Academic Article Autosomal dominant distal spinal muscular atrophy in four generations.
Academic Article Is the spinal muscular atrophy gene found?
Academic Article Progress toward cloning of the gene responsible for childhood spinal muscular atrophy.
Academic Article Genetic analysis of childhood-onset spinal muscular atrophy.
Academic Article Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locus.
Academic Article Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.
Academic Article Genetic mapping of chronic childhood-onset Spinal Muscular Atrophy to Chromosome 5q11.2-13.3
Search Criteria
  • Muscular Atrophy Spinal