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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

159 related items for PubMed ID: 8325895

  • 21.
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  • 22. Type II achondrogenesis-hypochondrogenesis: identification of abnormal type II collagen.
    Godfrey M, Hollister DW.
    Am J Hum Genet; 1988 Dec; 43(6):904-13. PubMed ID: 3195588
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  • 28. Type II procollagen gene (COL2A1) mutation in exon 11 associated with spondyloepiphyseal dysplasia, tall stature and precocious osteoarthritis.
    Bleasel JF, Bisagni-Faure A, Holderbaum D, Vacher-Lavenu MC, Haqqi TM, Moskowitz RW, Menkes CJ.
    J Rheumatol; 1995 Feb; 22(2):255-61. PubMed ID: 7738948
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  • 29. Novel amino acid substitution in the Y-position of collagen type II causes spondyloepimetaphyseal dysplasia congenita.
    Sulko J, Czarny-Ratajczak M, Wozniak A, Latos-Bielenska A, Kozlowski K.
    Am J Med Genet A; 2005 Sep 01; 137A(3):292-7. PubMed ID: 16088915
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  • 32. Lethal perinatal osteogenesis imperfecta due to a type I collagen alpha 2(I) Gly to Arg substitution detected by chemical cleavage of an mRNA:cDNA sequence mismatch.
    Bateman JF, Moeller I, Hannagan M, Chan D, Cole WG.
    Hum Mutat; 1992 Sep 01; 1(1):55-62. PubMed ID: 1284475
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  • 36. Osteogenesis imperfecta. The position of substitution for glycine by cysteine in the triple helical domain of the pro alpha 1(I) chains of type I collagen determines the clinical phenotype.
    Starman BJ, Eyre D, Charbonneau H, Harrylock M, Weis MA, Weiss L, Graham JM, Byers PH.
    J Clin Invest; 1989 Oct 01; 84(4):1206-14. PubMed ID: 2794057
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  • 38. A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation.
    Esapa CT, Hough TA, Testori S, Head RA, Crane EA, Chan CP, Evans H, Bassett JH, Tylzanowski P, McNally EG, Carr AJ, Boyde A, Howell PG, Clark A, Williams GR, Brown MA, Croucher PI, Nesbit MA, Brown SD, Cox RD, Cheeseman MT, Thakker RV.
    J Bone Miner Res; 2012 Feb 01; 27(2):413-28. PubMed ID: 22028304
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