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Richards, A. J., Baguley, D. M., Yates, J. R. W., Lane, C., Nicol, M., Harper, P. S., Scott, J. D., & Snead, M. P. (2000). Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helix. The American Journal of Human Genetics, 67, 1083-1094. doi:10.1086/321189

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