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Page 1
Anirdia-like phenotype caused by 6p25 dosage aberrations.
Sadagopan KA, Liu GT, Capasso JE, Wuthisiri W, Keep RB, Levin AV. Sadagopan KA, et al. Am J Med Genet A. 2015 Mar;167A(3):524-8. doi: 10.1002/ajmg.a.36890. Am J Med Genet A. 2015. PMID: 25691405
Ocular manifestations of 22q11.2 microduplication.
Cordovez JA, Capasso J, Lingao MD, Sadagopan KA, Spaeth GL, Wasserman BN, Levin AV. Cordovez JA, et al. Among authors: sadagopan ka. Ophthalmology. 2014 Jan;121(1):392-398. doi: 10.1016/j.ophtha.2013.06.040. Epub 2013 Aug 21. Ophthalmology. 2014. PMID: 23972321
Genetics for the ophthalmologist.
Sadagopan KA, Capasso J, Levin AV. Sadagopan KA, et al. Oman J Ophthalmol. 2012 Sep;5(3):144-9. doi: 10.4103/0974-620X.106092. Oman J Ophthalmol. 2012. PMID: 23439654 Free PMC article.
Organophosphate retinopathy.
Pham H, Lingao MD, Ganesh A, Capasso JE, Keep R, Sadagopan KA, Levin AV. Pham H, et al. Among authors: sadagopan ka. Oman J Ophthalmol. 2016 Jan-Apr;9(1):49-51. doi: 10.4103/0974-620X.176101. Oman J Ophthalmol. 2016. PMID: 27013829 Free PMC article.
Managing the patient with oculomotor nerve palsy.
Sadagopan KA, Wasserman BN. Sadagopan KA, et al. Curr Opin Ophthalmol. 2013 Sep;24(5):438-47. doi: 10.1097/ICU.0b013e3283645a9b. Curr Opin Ophthalmol. 2013. PMID: 23872817 Review.