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Masked confirmation of linkage between type 1 congenital vitreous anomaly and COL 2A1 in Stickler syndrome

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References

  1. Snead MP, Payne SJ, Barton DE, Yates JRW, Al-Imara L, Pope FM, Scott JD (1994) Stickler syndrome: correlation between vitreo-retinal phenotypes and linkage to COL 2A1. Eye 8:609–614

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  2. Vintiner GM, Temple IK, Middleton-Price HR, Baraitser M, Malcolm S (1991) Genetic and clinical heterogeneity of Stickler syndrome. Am J Med Genet 41: 44–48

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Authors and Affiliations

  1. Molecular Genetics Laboratory, Addenbrooke's NHS Trust, Hills Road, CB2 2QQ, Cambridge, UK

    Martin P. Snead

  2. Vitreo-retinal Unit, Department of Ophthalmology, Addenbrooke's NHS Trust, Hills Road, Box 41, CB2 2QQ, Cambridge, UK

    Martin P. Snead & John D. Scott

  3. Department of Clinical Genetics, Addenbrooke's NHS Trust, Hills Road, CB2 2QQ, Cambridge, UK

    John R. W. Yates

  4. Department of Pathology, University of Cambridge, Tennis Court Road, CB2 1QP, Cambridge, UK

    John R. W. Yates

  5. MRC Connective Tissue Genetics Group, Strangeways Research Laboratory, Worts Causeway, CB1 4RN, Cambridge, UK

    F. Michael Pope

  6. Department of Clinical Genetics, Southampton General Hospital, Tremona Road, S09 4XY, Southampton, UK

    I. Karen Temple

Authors
  1. Martin P. Snead
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  2. John R. W. Yates
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  3. F. Michael Pope
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  4. I. Karen Temple
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  5. John D. Scott
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Snead, M.P., Yates, J.R.W., Pope, F.M. et al. Masked confirmation of linkage between type 1 congenital vitreous anomaly and COL 2A1 in Stickler syndrome. Graefe's Arch Clin Exp Ophthalmol 234, 720–721 (1996). https://doi.org/10.1007/BF00292360

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  • DOI: https://doi.org/10.1007/BF00292360

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