Positional cloning with microsatellite markers allowed further localization of the Darier disease gene to a 2-cM interval of chromosome 12, 12q23-24.1, between the polymorphic loci D12S234 and D12S129. A region this size is suitable for construction of a contig to identify the Darier disease gene. Use of a polymorphic intronic marker for nitric oxide synthetase 1 gene, which maps to the same chromosomal area as the Darier gene, allowed exclusion of that gene as the Darier disease gene
We have recently described a family in which there is cosegregation of major affective disorder with...
Darier's disease is a rare autosomal dominantly inherited keratosis. This is an account of one famil...
Mutation analysis in the ATP2A2 gene had been performed in eight Hungarian patients with Darier's di...
Darier's disease (DD) is an autosomal dominant genodermatosis characterized by epidermal acantholysi...
Darier's disease is a dominantly inherited skin disorder in which there is abnormal adhesion between...
Darier disease is an autosomal dominant abnormality of epidermal differentiation characterized clini...
Medline is the source for the MeSH terms of this document.Darier disease (DD) (MIM 124200) is an aut...
Darier's disease is a rare autosomal dominant skin disorder in which there is abnormal adhesion betw...
Darier disease (DD) (MIM 124200) is an autosomaldominant skin disorder characterized by loss of adhe...
SIGLEAvailable from British Library Document Supply Centre-DSC:D206468 / BLDSC - British Library Doc...
Darier disease is a dominantly inherited skin disorder in which there appears to be abnormal adhesio...
SummaryDarier disease (DD) (MIM 124200) is an autosomal dominant skin disorder characterized by loss...
We developed a sequence-ready map of a part of human chromosome 12q24.1. We utilized a number of seq...
OBJECTIVE: The authors previously reported two families (pedigrees 324 and 5501) in which Darier’s d...
Munro and colleagues (Ann Génét, 1992, 35, 157-160) found small positive lod scores for linkage betw...
We have recently described a family in which there is cosegregation of major affective disorder with...
Darier's disease is a rare autosomal dominantly inherited keratosis. This is an account of one famil...
Mutation analysis in the ATP2A2 gene had been performed in eight Hungarian patients with Darier's di...
Darier's disease (DD) is an autosomal dominant genodermatosis characterized by epidermal acantholysi...
Darier's disease is a dominantly inherited skin disorder in which there is abnormal adhesion between...
Darier disease is an autosomal dominant abnormality of epidermal differentiation characterized clini...
Medline is the source for the MeSH terms of this document.Darier disease (DD) (MIM 124200) is an aut...
Darier's disease is a rare autosomal dominant skin disorder in which there is abnormal adhesion betw...
Darier disease (DD) (MIM 124200) is an autosomaldominant skin disorder characterized by loss of adhe...
SIGLEAvailable from British Library Document Supply Centre-DSC:D206468 / BLDSC - British Library Doc...
Darier disease is a dominantly inherited skin disorder in which there appears to be abnormal adhesio...
SummaryDarier disease (DD) (MIM 124200) is an autosomal dominant skin disorder characterized by loss...
We developed a sequence-ready map of a part of human chromosome 12q24.1. We utilized a number of seq...
OBJECTIVE: The authors previously reported two families (pedigrees 324 and 5501) in which Darier’s d...
Munro and colleagues (Ann Génét, 1992, 35, 157-160) found small positive lod scores for linkage betw...
We have recently described a family in which there is cosegregation of major affective disorder with...
Darier's disease is a rare autosomal dominantly inherited keratosis. This is an account of one famil...
Mutation analysis in the ATP2A2 gene had been performed in eight Hungarian patients with Darier's di...