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Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromes.Academic Article Why?
Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.Academic Article Why?
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity.Academic Article Why?
Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease.Academic Article Why?
Genetic heterogeneity of inherited cerebral cavernous malformation.Academic Article Why?
An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy.Academic Article Why?
Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.Academic Article Why?
Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency: evidence for genetic heterogeneity.Academic Article Why?
Genetic heterogeneity in colorectal cancer associations between African and European americans.Academic Article Why?
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.Academic Article Why?
Genetic HeterogeneityConcept Why?
Chromosome arm 17p deletion analysis reveals molecular genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumors of the central nervous system.Academic Article Why?
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity.Academic Article Why?
Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere.Academic Article Why?
Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression.Academic Article Why?
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