Blue sclera with and without corneal fragility (brittle cornea syndrome) in a consanguineous family harboring ZNF469 mutation (p.E1392X).

MLA

Khan, Arif O., et al. “Blue Sclera with and without Corneal Fragility (Brittle Cornea Syndrome) in a Consanguineous Family Harboring ZNF469 Mutation (p.E1392X).” Archives of Ophthalmology (Chicago, Ill. : 1960), vol. 128, no. 10, Oct. 2010, pp. 1376–79. EBSCOhost, https://doi.org/10.1001/archophthalmol.2010.238.

APA

Khan, A. O., Aldahmesh, M. A., Mohamed, J. N., & Alkuraya, F. S. (2010). Blue sclera with and without corneal fragility (brittle cornea syndrome) in a consanguineous family harboring ZNF469 mutation (p.E1392X). Archives of Ophthalmology (Chicago, Ill. : 1960), 128(10), 1376–1379. https://doi.org/10.1001/archophthalmol.2010.238

Chicago

Khan, Arif O, Mohammed A Aldahmesh, Jawahir N Mohamed, and Fowzan S Alkuraya. 2010. “Blue Sclera with and without Corneal Fragility (Brittle Cornea Syndrome) in a Consanguineous Family Harboring ZNF469 Mutation (p.E1392X).” Archives of Ophthalmology (Chicago, Ill. : 1960) 128 (10): 1376–79. doi:10.1001/archophthalmol.2010.238.