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Journal Abstract Search

143 related items for PubMed ID: 2902229

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  • 3. Evidence against the structural gene encoding type II collagen (COL2A1) as the mutant locus in achondroplasia.
    Ogilvie D, Wordsworth P, Thompson E, Sykes B.
    J Med Genet; 1986 Feb; 23(1):19-22. PubMed ID: 3005580
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  • 6. The Stickler syndrome: evidence for close linkage to the structural gene for type II collagen.
    Francomano CA, Liberfarb RM, Hirose T, Maumenee IH, Streeten EA, Meyers DA, Pyeritz RE.
    Genomics; 1987 Dec; 1(4):293-6. PubMed ID: 2896625
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  • 8. Molecular genetic basis of the human chondrodysplasias.
    Horton WA.
    Endocrinol Metab Clin North Am; 1996 Sep; 25(3):683-97. PubMed ID: 8879993
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  • 11. Segregation of structural collagen genes in adolescent idiopathic scoliosis.
    Carr AJ, Ogilvie DJ, Wordsworth BP, Priestly LM, Smith R, Sykes B.
    Clin Orthop Relat Res; 1992 Jan; (274):305-10. PubMed ID: 1345899
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  • 12. Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneity.
    Gertner JM, Whyte MP, Dixon PH, Pang JT, Trump D, Pearce SH, Wooding C, Thakker RV.
    J Bone Miner Res; 1997 Aug; 12(8):1204-9. PubMed ID: 9258750
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  • 13. Exclusion of human proteoglycan link protein (CRTL1) and type II collagen (COL2A1) genes in pseudoachondroplasia.
    Hecht JT, Blanton SH, Wang Y, Daiger SP, Horton WA, Rhodes C, Yamada Y, Francomano CA.
    Am J Med Genet; 1992 Nov 01; 44(4):420-4. PubMed ID: 1442879
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  • 15. Exclusion of the alpha 1(II) collagen structural gene as the mutant locus in type II Ehlers-Danlos syndrome.
    Wordsworth P, Ogilvie D, Smith R, Sykes B.
    Ann Rheum Dis; 1985 Jul 01; 44(7):431-3. PubMed ID: 2992397
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  • 16. Spondyloepiphyseal dysplasia in a Cape Town family: linkage with the gene for type II collagen (COL2A1).
    Ramesar R, Beighton P.
    Am J Med Genet; 1992 Jul 15; 43(5):833-8. PubMed ID: 1353665
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  • 17. SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia.
    Sweetman WA, Rash B, Sykes B, Beighton P, Hecht JT, Zabel B, Thomas JT, Boot-Handford R, Grant ME, Wallis GA.
    Am J Hum Genet; 1992 Oct 15; 51(4):841-9. PubMed ID: 1329505
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  • 19. Strategy for prenatal diagnosis of osteogenesis imperfecta by linkage analysis to the type I collagen loci COL1A1 and COL1A2.
    Benušienė E, Kučinskas V.
    Med Sci Monit; 2000 Oct 15; 6(2):217-26. PubMed ID: 11208313
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  • 20. Heritable diseases of cartilage caused by mutations in collagen genes.
    Williams CJ, Jimenez SA.
    J Rheumatol Suppl; 1995 Feb 15; 43():28-33. PubMed ID: 7752129
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