SummaryDarier disease (DD) (MIM 124200) is an autosomal dominant skin disorder characterized by loss of adhesion between epidermal cells and by abnormal keratinization. We present linkage analysis showing, in four families, key recombination events that refine the location of the DD locus on chromosome 12q23-24.1 to a region of <1 cM. We have constructed a YAC/P1 artificial chromosome (PAC)/bacterial artificial chromosome (BAC)–based physical map that encompasses this refined DD region. The map consists of 35 YAC, 69 PAC, 16 BAC, and 2 cosmid clones that were ordered by mapping 54 anonymous sequence-tagged sites. The critical region is estimated to be 2.4 Mb in size, with an average marker resolution of 37.5 kb. The refinement of the critic...
Darier disease (DD) is an autosomal-dominant skin disorder characterized by loss of adhesion between...
Clouston hidrotic ectodermal dysplasia (BED) is an autosomal dominant skin disorder that is characte...
SummaryHuman genomic DNA containing two type II keratin genes, one coding for keratin 1 (K1, a 68-kD...
SummaryDarier disease (DD) (MIM 124200) is an autosomal dominant skin disorder characterized by loss...
Darier disease (DD) (MIM 124200) is an autosomaldominant skin disorder characterized by loss of adhe...
Medline is the source for the MeSH terms of this document.Darier disease (DD) (MIM 124200) is an aut...
Darier's disease (DD) is an autosomal dominant genodermatosis characterized by epidermal acantholysi...
Darier disease is an autosomal dominant abnormality of epidermal differentiation characterized clini...
Darier's disease is a dominantly inherited skin disorder in which there is abnormal adhesion between...
Darier's disease is a rare autosomal dominant skin disorder in which there is abnormal adhesion betw...
Dyschromatosis symmetrica hereditaria is a rare autosomal dominant cutaneous disorder characterized ...
Darier disease is a dominantly inherited skin disorder in which there appears to be abnormal adhesio...
The epidermal differentiation complex (EDC) unites a remarkable number of structurally, functionally...
Terminal differentiation of keratinocytes involves the sequential expression of several major protei...
Disseminated superficial porokeratosis (DSP) is a rare autosomal dominant epidermal keratinization d...
Darier disease (DD) is an autosomal-dominant skin disorder characterized by loss of adhesion between...
Clouston hidrotic ectodermal dysplasia (BED) is an autosomal dominant skin disorder that is characte...
SummaryHuman genomic DNA containing two type II keratin genes, one coding for keratin 1 (K1, a 68-kD...
SummaryDarier disease (DD) (MIM 124200) is an autosomal dominant skin disorder characterized by loss...
Darier disease (DD) (MIM 124200) is an autosomaldominant skin disorder characterized by loss of adhe...
Medline is the source for the MeSH terms of this document.Darier disease (DD) (MIM 124200) is an aut...
Darier's disease (DD) is an autosomal dominant genodermatosis characterized by epidermal acantholysi...
Darier disease is an autosomal dominant abnormality of epidermal differentiation characterized clini...
Darier's disease is a dominantly inherited skin disorder in which there is abnormal adhesion between...
Darier's disease is a rare autosomal dominant skin disorder in which there is abnormal adhesion betw...
Dyschromatosis symmetrica hereditaria is a rare autosomal dominant cutaneous disorder characterized ...
Darier disease is a dominantly inherited skin disorder in which there appears to be abnormal adhesio...
The epidermal differentiation complex (EDC) unites a remarkable number of structurally, functionally...
Terminal differentiation of keratinocytes involves the sequential expression of several major protei...
Disseminated superficial porokeratosis (DSP) is a rare autosomal dominant epidermal keratinization d...
Darier disease (DD) is an autosomal-dominant skin disorder characterized by loss of adhesion between...
Clouston hidrotic ectodermal dysplasia (BED) is an autosomal dominant skin disorder that is characte...
SummaryHuman genomic DNA containing two type II keratin genes, one coding for keratin 1 (K1, a 68-kD...