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Spectrum of PEX1 and PEX6 variants in Heimler syndrome.
Smith CE, Poulter JA, Levin AV, Capasso JE, Price S, Ben-Yosef T, Sharony R, Newman WG, Shore RC, Brookes SJ, Mighell AJ, Inglehearn CF. Smith CE, et al. Among authors: capasso je. Eur J Hum Genet. 2016 Nov;24(11):1565-1571. doi: 10.1038/ejhg.2016.62. Epub 2016 Jun 15. Eur J Hum Genet. 2016. PMID: 27302843 Free PMC article.
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.
Lyonization in ophthalmology.
Wuthisiri W, Lingao MD, Capasso JE, Levin AV. Wuthisiri W, et al. Among authors: capasso je. Curr Opin Ophthalmol. 2013 Sep;24(5):389-97. doi: 10.1097/ICU.0b013e3283641f91. Curr Opin Ophthalmol. 2013. PMID: 23892913 Review.
Ocular manifestations of 22q11.2 microduplication.
Cordovez JA, Capasso J, Lingao MD, Sadagopan KA, Spaeth GL, Wasserman BN, Levin AV. Cordovez JA, et al. Ophthalmology. 2014 Jan;121(1):392-398. doi: 10.1016/j.ophtha.2013.06.040. Epub 2013 Aug 21. Ophthalmology. 2014. PMID: 23972321
Anirdia-like phenotype caused by 6p25 dosage aberrations.
Sadagopan KA, Liu GT, Capasso JE, Wuthisiri W, Keep RB, Levin AV. Sadagopan KA, et al. Among authors: capasso je. 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
Peters anomaly in cri-du-chat syndrome.
Hope WC, Cordovez JA, Capasso JE, Hammersmith KM, Eagle RC, Lall-Trail J, Levin AV. Hope WC, et al. Among authors: capasso je. J AAPOS. 2015 Jun;19(3):277-9. doi: 10.1016/j.jaapos.2015.01.018. J AAPOS. 2015. PMID: 26059676
40 results