Autosomal dominant spondyloarthropathy: no linkage to the type II collagen gene.

Autosomal Dominant Osteopetrosis Type II.

Spondyloepiphyseal dysplasia, mild autosomal dominant type is not due to primary defects of type II collagen.

Mild spondyloepiphyseal dysplasia (Namaqualand type): genetic linkage to the type II collagen gene COL2A1.

Spondyloepiphyseal dysplasia congenita: genetic linkage to type II collagen (COL2AI).

Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3.

Human type VII collagen: genetic linkage of the gene (COL7A1) on chromosome 3 to dominant dystrophic epidermolysis bullosa.

Spondyloepiphyseal dysplasia in a Cape Town family: linkage with the gene for type II collagen (COL2A1).

Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q.

Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneity.

Genetic linkage between the collagen VII (COL7A1) gene and the autosomal dominant form of dystrophic epidermolysis bullosa in two Dutch kindreds.

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene.

Generation of the first autosomal dominant osteopetrosis type II (ADO2) disease models.

No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palate.

Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family.

Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq.

Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13.

Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case Report.

Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1.

Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils.

Elevated serum levels of creatine kinase BB in autosomal dominant osteopetrosis type II.

Elevated serum levels of creatine kinase BB in autosomal dominant osteopetrosis type II--a family study.

Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locus.

Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q.

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Autosomal Dominant Osteopetrosis Type II.

Spondyloepiphyseal dysplasia, mild autosomal dominant type is not due to primary defects of type II collagen.

Mild spondyloepiphyseal dysplasia (Namaqualand type): genetic linkage to the type II collagen gene COL2A1.

Spondyloepiphyseal dysplasia congenita: genetic linkage to type II collagen (COL2AI).

Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3.

Human type VII collagen: genetic linkage of the gene (COL7A1) on chromosome 3 to dominant dystrophic epidermolysis bullosa.

Spondyloepiphyseal dysplasia in a Cape Town family: linkage with the gene for type II collagen (COL2A1).

Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q.

Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneity.

Genetic linkage between the collagen VII (COL7A1) gene and the autosomal dominant form of dystrophic epidermolysis bullosa in two Dutch kindreds.

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene.

Generation of the first autosomal dominant osteopetrosis type II (ADO2) disease models.

No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palate.

Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family.

Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq.

Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13.

Clinical and Radiological Findings of Autosomal Dominant Osteopetrosis Type II: A Case Report.

Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1.

Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils.

Elevated serum levels of creatine kinase BB in autosomal dominant osteopetrosis type II.

Elevated serum levels of creatine kinase BB in autosomal dominant osteopetrosis type II--a family study.

Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locus.

Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q.

Autosomal dominant spondyloarthropathy: no linkage to the type II collagen gene.

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