Darier disease is a dominantly inherited skin disorder in which there appears to be abnormal adhesion between keratinocytes. We and others have shown that the disease in some British pedigrees is closely linked to markers mapping to 12q23-q24.1. In the present study we have defined crossovers that enable us to narrow the location of the disease gene to the interval between the D12S105 and the D12S129 markers. This interval may be expected to be on the order of about 4 cM on the basis of linkage data obtained using the primary CEPH reference families. Our data provide further evidence for locus homogeneity: each of four large British pedigrees, two of which have previously been subjected to preliminary characterization, shows statistically s...
OBJECTIVE: The authors previously reported two families (pedigrees 324 and 5501) in which Darier’s d...
The introduction of recombinant DNA technology has led to the isolation of a number of neurological ...
Idiopathic torsion dystonia is most commonly caused by an autosomal dominant gene or genes with redu...
Darier's disease is a rare autosomal dominant skin disorder in which there is abnormal adhesion betw...
Darier's disease is a dominantly inherited skin disorder in which there is abnormal adhesion between...
Darier's disease (DD) is an autosomal dominant genodermatosis characterized by epidermal acantholysi...
Munro and colleagues (Ann Génét, 1992, 35, 157-160) found small positive lod scores for linkage betw...
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 dominantly inherited keratosis. This is an account of one famil...
Darier disease (DD) (MIM 124200) is an autosomaldominant skin disorder characterized by loss of adhe...
SummaryDarier disease (DD) (MIM 124200) is an autosomal dominant skin disorder characterized by loss...
Darier's disease is a rare autosomal dominantly inherited keratosis.1 We have previously reported a ...
We have recently described a family in which there is cosegregation of major affective disorder with...
Positional cloning with microsatellite markers allowed further localization of the Darier disease ge...
OBJECTIVE: The authors previously reported two families (pedigrees 324 and 5501) in which Darier’s d...
The introduction of recombinant DNA technology has led to the isolation of a number of neurological ...
Idiopathic torsion dystonia is most commonly caused by an autosomal dominant gene or genes with redu...
Darier's disease is a rare autosomal dominant skin disorder in which there is abnormal adhesion betw...
Darier's disease is a dominantly inherited skin disorder in which there is abnormal adhesion between...
Darier's disease (DD) is an autosomal dominant genodermatosis characterized by epidermal acantholysi...
Munro and colleagues (Ann Génét, 1992, 35, 157-160) found small positive lod scores for linkage betw...
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 dominantly inherited keratosis. This is an account of one famil...
Darier disease (DD) (MIM 124200) is an autosomaldominant skin disorder characterized by loss of adhe...
SummaryDarier disease (DD) (MIM 124200) is an autosomal dominant skin disorder characterized by loss...
Darier's disease is a rare autosomal dominantly inherited keratosis.1 We have previously reported a ...
We have recently described a family in which there is cosegregation of major affective disorder with...
Positional cloning with microsatellite markers allowed further localization of the Darier disease ge...
OBJECTIVE: The authors previously reported two families (pedigrees 324 and 5501) in which Darier’s d...
The introduction of recombinant DNA technology has led to the isolation of a number of neurological ...
Idiopathic torsion dystonia is most commonly caused by an autosomal dominant gene or genes with redu...