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Retinal Development and Pathophysiology in Kcnj13 Knockout Mice.
Jiao X, Ma Z, Lei J, Liu P, Cai X, Shahi PK, Chan CC, Fariss R, Pattnaik BR, Dong L, Hejtmancik JF. Jiao X, et al. Among authors: fariss r. Front Cell Dev Biol. 2022 Jan 12;9:810020. doi: 10.3389/fcell.2021.810020. eCollection 2021. Front Cell Dev Biol. 2022. PMID: 35096838 Free PMC article.
Mutations in FYCO1 cause autosomal-recessive congenital cataracts.
Chen J, Ma Z, Jiao X, Fariss R, Kantorow WL, Kantorow M, Pras E, Frydman M, Pras E, Riazuddin S, Riazuddin SA, Hejtmancik JF. Chen J, et al. Among authors: fariss r. Am J Hum Genet. 2011 Jun 10;88(6):827-838. doi: 10.1016/j.ajhg.2011.05.008. Am J Hum Genet. 2011. PMID: 21636066 Free PMC article.
Waldenström's macroglobulinemia-associated retinopathy.
Sen HN, Chan CC, Caruso RC, Fariss RN, Nussenblatt RB, Buggage RR. Sen HN, et al. Among authors: fariss rn. Ophthalmology. 2004 Mar;111(3):535-9. doi: 10.1016/j.ophtha.2003.05.036. Ophthalmology. 2004. PMID: 15019332
132 results