This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to
Kerrison, John
Item Type | Name |
Concept
|
Chromosomes, Human, Pair 7
|
Concept
|
Chromosomes, Human, Pair 6
|
Concept
|
Chromosomes, Human, Pair 18
|
Concept
|
Chromosomes, Human, Pair 15
|
Concept
|
Chromosomes, Human, Pair 3
|
Concept
|
Chromosome Mapping
|
Concept
|
X Chromosome
|
Academic Article
|
A gene for autosomal dominant congenital nystagmus localizes to 6p12.
|
Academic Article
|
Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12.
|
Academic Article
|
Congenital motor nystagmus linked to Xq26-q27.
|
Academic Article
|
Novel mutations in FRMD7 in X-linked congenital nystagmus. Mutation in brief #963. Online.
|
Academic Article
|
Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3.
|
Academic Article
|
Hereditary optic neuropathies.
|
Academic Article
|
Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1).
|