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Ocular findings in the chromosome 22q11.2 deletion syndrome.
Forbes BJ, Binenbaum G, Edmond JC, DeLarato N, McDonald-McGinn DM, Zackai EH. Forbes BJ, et al. J AAPOS. 2007 Apr;11(2):179-82. doi: 10.1016/j.jaapos.2006.08.006. Epub 2006 Nov 30. J AAPOS. 2007. PMID: 17140829
Sclerocornea associated with the chromosome 22q11.2 deletion syndrome.
Binenbaum G, McDonald-McGinn DM, Zackai EH, Walker BM, Coleman K, Mach AM, Adam M, Manning M, Alcorn DM, Zabel C, Anderson DR, Forbes BJ. Binenbaum G, et al. Among authors: forbes bj. Am J Med Genet A. 2008 Apr 1;146A(7):904-9. doi: 10.1002/ajmg.a.32156. Am J Med Genet A. 2008. PMID: 18324686 Free PMC article.
Central corneal thickness in children.
Pediatric Eye Disease Investigator Group; Bradfield YS, Melia BM, Repka MX, Kaminski BM, Davitt BV, Johnson DA, Kraker RT, Manny RE, Matta NS, Weise KK, Schloff S. Pediatric Eye Disease Investigator Group, et al. Arch Ophthalmol. 2011 Sep;129(9):1132-8. doi: 10.1001/archophthalmol.2011.225. Arch Ophthalmol. 2011. PMID: 21911662 Free PMC article.
447 results