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X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development.
Webb TR, Matarin M, Gardner JC, Kelberman D, Hassan H, Ang W, Michaelides M, Ruddle JB, Pennell CE, Yazar S, Khor CC, Aung T, Yogarajah M, Robson AG, Holder GE, Cheetham ME, Traboulsi EI, Moore AT, Sowden JC, Sisodiya SM, Mackey DA, Tuft SJ, Hardcastle AJ. Webb TR, et al. Among authors: mackey da. Am J Hum Genet. 2012 Feb 10;90(2):247-59. doi: 10.1016/j.ajhg.2011.12.019. Epub 2012 Jan 26. Am J Hum Genet. 2012. PMID: 22284829 Free PMC article.
Birth of a cohort--the first 20 years of the Raine study.
McKnight CM, Newnham JP, Stanley FJ, Mountain JA, Landau LI, Beilin LJ, Puddey IB, Pennell CE, Mackey DA. McKnight CM, et al. Among authors: mackey da. Med J Aust. 2012 Dec 10;197(11):608-10. doi: 10.5694/mja12.10698. Med J Aust. 2012. PMID: 23230915 No abstract available.
Raine eye health study: design, methodology and baseline prevalence of ophthalmic disease in a birth-cohort study of young adults.
Yazar S, Forward H, McKnight CM, Tan A, Soloshenko A, Oates SK, Ang W, Sherwin JC, Wood D, Mountain JA, Pennell CE, Hewitt AW, Mackey DA. Yazar S, et al. Among authors: mackey da. Ophthalmic Genet. 2013 Dec;34(4):199-208. doi: 10.3109/13816810.2012.755632. Epub 2013 Jan 10. Ophthalmic Genet. 2013. PMID: 23301674 Free article. Clinical Trial.
550 results