Genetic linkage of a polymorphism in the type II procollagen gene (COL2A1) to primary osteoarthritis associated with mild chondrodysplasia.

Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia.

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

Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasia.

PCR detection of a HindIII polymorphism in the human gene for type II procollagen (COL2A1).

Cartilage expression of a type II collagen mutation in an inherited form of osteoarthritis associated with a mild chondrodysplasia.

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

Human collagen, type II, alpha 1, (COL2A1) gene: VNTR polymorphism detected by gene amplification.

Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy).

A glycine to serine polymorphism in the C-propeptide of the human type II procollagen.

Tandem duplication within a type II collagen gene (COL2A1) exon in an individual with spondyloepiphyseal dysplasia.

Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene.

Association of COL2A1 gene polymorphism with degenerative lumbar scoliosis.

Linkage disequilibrium between two restriction sites in the COL2A1 gene.

ADAMTS14 gene polymorphism associated with knee osteoarthritis in Thai women.

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

Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1.

Characterization of a type II collagen gene (COL2A1) mutation identified in cultured chondrocytes from human hypochondrogenesis.

Detection of sequence variants in the gene for human type II procollagen (COL2A1) by direct sequencing of polymerase chain reaction-amplified genomic DNA.

Completion of the intron-exon structure of the gene for human type II procollagen (COL2A1): variations in the nucleotide sequences of the alleles from three chromosomes.

Mutation in the type II collagen gene (COL2A1) as a cause of early osteoarthritis and juvenile idiopathic arthritis-A pseudorheumatoid arthritis variant.

Procollagen II gene mutation in Stickler syndrome.

Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene.

[EXPRESS] Single Nucleotide Polymorphism in the COL11A2 Gene Associated with Heat Pain Sensitivity in Knee Osteoarthritis.

Novel functions for type II procollagen.

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Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia.

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

Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasia.

PCR detection of a HindIII polymorphism in the human gene for type II procollagen (COL2A1).

Cartilage expression of a type II collagen mutation in an inherited form of osteoarthritis associated with a mild chondrodysplasia.

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

Human collagen, type II, alpha 1, (COL2A1) gene: VNTR polymorphism detected by gene amplification.

Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy).

A glycine to serine polymorphism in the C-propeptide of the human type II procollagen.

Tandem duplication within a type II collagen gene (COL2A1) exon in an individual with spondyloepiphyseal dysplasia.

Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene.

Association of COL2A1 gene polymorphism with degenerative lumbar scoliosis.

Linkage disequilibrium between two restriction sites in the COL2A1 gene.

ADAMTS14 gene polymorphism associated with knee osteoarthritis in Thai women.

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

Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1.

Characterization of a type II collagen gene (COL2A1) mutation identified in cultured chondrocytes from human hypochondrogenesis.

Detection of sequence variants in the gene for human type II procollagen (COL2A1) by direct sequencing of polymerase chain reaction-amplified genomic DNA.

Completion of the intron-exon structure of the gene for human type II procollagen (COL2A1): variations in the nucleotide sequences of the alleles from three chromosomes.

Mutation in the type II collagen gene (COL2A1) as a cause of early osteoarthritis and juvenile idiopathic arthritis-A pseudorheumatoid arthritis variant.

Procollagen II gene mutation in Stickler syndrome.

Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene.

[EXPRESS] Single Nucleotide Polymorphism in the COL11A2 Gene Associated with Heat Pain Sensitivity in Knee Osteoarthritis.

Novel functions for type II procollagen.

Genetic linkage of a polymorphism in the type II procollagen gene (COL2A1) to primary osteoarthritis associated with mild chondrodysplasia.

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