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Letters to the Journal

Megalocornea associated with microduplications on chromosome 16

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References

  • Davidson AE, Cheong SS, Hysi PG, et al. Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhauser syndrome and central corneal thickness. PLoS One 2014;9:e104163.
  • Desir J, Sznajer Y, Depasse F, et al. LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma. Europ J Hum Genet 2010;18:761–767.
  • Frank Y, Ziprkowski M, Romano A, et al. Megalocornea associated with multiple skeletal anomalies: a new genetic syndrome? J Genet Hum 1973;21:67–72.
  • Rosser EM, Mann NP, Hall CM, et al. Serpentine fibula syndrome: expansion of the phenotype with three affected siblings. Clin Dysmorph 1996;5:105–113.
  • Schwingshandl J, Mache CJ, Rath K, et al. SHORT syndrome and insulin resistance. Am J Med Genet 1993;47:907–909.
  • Christensen AE, Knappskog PM, Midtbo M, et al. Brittle cornea syndrome associated with a missense mutation in the zinc-finger 469 gene. Invest Ophthal Vis Sci 2010;51:47–52.

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