Tuberous sclerosis complex (TSC) is an autosomal dominant disorder of unknown aetiology that affects numerous body systems including skin, brain and kidneys. Some TSC has been linked to chromosome 9, additional TSC genes on chromosomes 11 and 12 have been proposed, but the majority of TSC families remain unlinked. Using TSC families in which data had excluded linkage to chromosome 9, we failed to detect linkage with loci on chromosomes 11, 12 and others. One marker examined was D16S283, the closest locus on the proximal side of the polycystic kidney disease type 1 (PKD1) gene. Linkage between TSC and D16S283 demonstrated a lod score of 9.50 at theta = 0.02 with one family independently presenting a lod score of 4.44 at theta = 0.05. These d...
Tuberous sclerosis (TSC) is an autosomal dominant disorder characterised by the development of hamar...
Tuberous Sclerosis (TSC) is an autosomal dominant disorder with a prevalence of 1 in 10,000 births. ...
textabstractWe report on a familial submicroscopic translocation involving chromosomes 8 and ...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder of unknown aetiology that affects...
Tuberous sclerosis (TSC) is a dominantly inherited disorder characterized by hamartomas and hamartia...
Tuberous sclerosis is a dominantly inherited genetic disorder, with a high frequency of new mutation...
SummaryTuberous sclerosis is an autosomal dominant trait characterized by the development of hamarto...
Tuberous sclerosis is an autosomal dominant trait characterized by the development of hamartomatous ...
Tuberous sclerosis(TS) is an autosomal dominant disease caused by mutations in TSC1 and TSC2 genes. ...
textabstractTuberous sclerosis (TSC) is a heterogeneous trait. Since 1990, linkage studies have yiel...
Tuberous sclerosis (TSC) is an autosomal dominant multisystem disorder with loci assigned to chromos...
Tuberous sclerosis (TSC) is an autosomal dominant disorder characterized by hamartomas in one or mor...
Tuberous sclerosis (TSC) is an autosomal dominant condition with characteristic skin lesions, mental...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder with a great degree of phenotypic...
Tuberous sclerosis is an inherited disease typically characterised by a facial rash, seizures and me...
Tuberous sclerosis (TSC) is an autosomal dominant disorder characterised by the development of hamar...
Tuberous Sclerosis (TSC) is an autosomal dominant disorder with a prevalence of 1 in 10,000 births. ...
textabstractWe report on a familial submicroscopic translocation involving chromosomes 8 and ...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder of unknown aetiology that affects...
Tuberous sclerosis (TSC) is a dominantly inherited disorder characterized by hamartomas and hamartia...
Tuberous sclerosis is a dominantly inherited genetic disorder, with a high frequency of new mutation...
SummaryTuberous sclerosis is an autosomal dominant trait characterized by the development of hamarto...
Tuberous sclerosis is an autosomal dominant trait characterized by the development of hamartomatous ...
Tuberous sclerosis(TS) is an autosomal dominant disease caused by mutations in TSC1 and TSC2 genes. ...
textabstractTuberous sclerosis (TSC) is a heterogeneous trait. Since 1990, linkage studies have yiel...
Tuberous sclerosis (TSC) is an autosomal dominant multisystem disorder with loci assigned to chromos...
Tuberous sclerosis (TSC) is an autosomal dominant disorder characterized by hamartomas in one or mor...
Tuberous sclerosis (TSC) is an autosomal dominant condition with characteristic skin lesions, mental...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder with a great degree of phenotypic...
Tuberous sclerosis is an inherited disease typically characterised by a facial rash, seizures and me...
Tuberous sclerosis (TSC) is an autosomal dominant disorder characterised by the development of hamar...
Tuberous Sclerosis (TSC) is an autosomal dominant disorder with a prevalence of 1 in 10,000 births. ...
textabstractWe report on a familial submicroscopic translocation involving chromosomes 8 and ...