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Science (New York, N.Y.)|July 20, 1999

An allele of COL9A2 associated with intervertebral disc diseaseS Annunen, P Paassilta, J Lohiniva, et al.

Calcified Tissue International|May 28, 2005

Abnormal response to physical activity in femurs after heterozygous inactivation of one allele of the Col2a1 gene for type II collagen in miceJ Nieminen, J Sahlman, T Hirvonen, et al.

Development (Cambridge, England)|November 15, 2000

Papilin in development; a pericellular protein with a homology to the ADAMTS metalloproteinasesI A Kramerova, N Kawaguchi, L I Fessler, et al.

American Journal of Human Genetics|July 27, 1999

Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase geneA Colige, A L Sieron, S W Li, et al.

European Journal of Human Genetics : EJHG|October 22, 1998

First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4qM Devoto, K Shimoya, J Caminis, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 1, 1982

Human type I procollagen genes are located on different chromosomesC Huerre, C Junien, D Weil, et al.

Immunology|January 20, 1999

Characterization of recombinant type II collagen: arthritogenicity and tolerogenicity in DBA/1 miceL K Myers, D D Brand, X J Ye, et al.

American Journal of Human Genetics|January 23, 1999

Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition diseaseL J Andrew, V Brancolini, L S de la Pena, et al.

Nature Genetics|December 2, 1999

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.

American Journal of Human Genetics|September 16, 1999

Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypesS Annunen, J Körkkö, M Czarny, et al.

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Showing results (261-270 of 270) with videos related to

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Pageof 27

You have reached the last page of results.This site can display upto 270 results.

Science (New York, N.Y.)|July 20, 1999

An allele of COL9A2 associated with intervertebral disc diseaseS Annunen, P Paassilta, J Lohiniva, et al.

Calcified Tissue International|May 28, 2005

Abnormal response to physical activity in femurs after heterozygous inactivation of one allele of the Col2a1 gene for type II collagen in miceJ Nieminen, J Sahlman, T Hirvonen, et al.

Development (Cambridge, England)|November 15, 2000

Papilin in development; a pericellular protein with a homology to the ADAMTS metalloproteinasesI A Kramerova, N Kawaguchi, L I Fessler, et al.

American Journal of Human Genetics|July 27, 1999

Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase geneA Colige, A L Sieron, S W Li, et al.

European Journal of Human Genetics : EJHG|October 22, 1998

First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4qM Devoto, K Shimoya, J Caminis, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 1, 1982

Human type I procollagen genes are located on different chromosomesC Huerre, C Junien, D Weil, et al.

Immunology|January 20, 1999

Characterization of recombinant type II collagen: arthritogenicity and tolerogenicity in DBA/1 miceL K Myers, D D Brand, X J Ye, et al.

American Journal of Human Genetics|January 23, 1999

Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition diseaseL J Andrew, V Brancolini, L S de la Pena, et al.

Nature Genetics|December 2, 1999

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.

American Journal of Human Genetics|September 16, 1999

Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypesS Annunen, J Körkkö, M Czarny, et al.

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