Mutation of a nuclear receptor gene, NR2E3 , causes enhanced S cone syndrome, a disorder of retinal cell fate von Sheffield, Val C, Carmi, Rivka, Hockey, Robin, Haider, Neena B, Searby, Charles, Cideciyan, Artur V, Gorman, Susan, Streb, Luan M, Stone, Edwin M, Wright, Alan F, Hanna, David B, Swiderski, Ruth, Jacobson, Samuel G, Fishman, Gerald A, Bennett, Jean, Duhl, David, Beck, Gretel, Weleber, Richard G

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Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration von Sheffield, Val C, Stone, Edwin M, Streb, Luan M, Hockey, Robin R, Lotery, Andrew J, Webster, Andrew R, Vandenburgh, Kimberlie

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Phenotypic heterogeneity associated with a novel mutation (Gly112Glu) in the Norrie disease protein von Allen, R C, Russell, S R, Streb, L M, Alsheikheh, A, Stone, E M

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Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31 von Sheffield, Val C, Stone, Edwin M, Alward, Wallace L.M, Drack, Arlene V, Johnson, A. Tim, Streb, Luan M, Nichols, Brian E

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Three autosomal dominant corneal dystrophies map to chromosome 5q von Stone, Edwin M, Mathers, William D, Rosenwasser, George O.D, Holland, Edward J, Folberg, Robert, Krachmer, Jay H, Nichols, Brian E, Gorevic, Peter D, Taylor, Chris M, Streb, Luan M, Fishbaugh, Jill A, Daley, Thomas E, Sucheski, Brian M, Sheffield, Val C

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Minna Citron's "Feminanities": Her Commentary on the Culture of Vanity von Streb, Jennifer L.

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Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13 von Stone, Edwin M, Nichols, Brian E, Streb, Luan M, Kimura, Alan E, Sheffield, Val C

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Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25) von Héon, Elise, Sheth, Bhavna P., Kalenak, Jeffrey W., Sunden, Sara L.F., Streb, Luan M., Taylor, Chris M., Alward, Wallace L.M., C.Sheffield, Val, Stone, Edwin M.

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Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13 von Stone, Edwin M., Kimura, Alan E., Folk, James C., Bennett, Steven R., Nichols, Brian E., Streb, Luan M., Sheffield, Val C.

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Genotype-phenotype correlation in a family with Arg135Leu rhodopsin retinitis pigmentosa von Oh, K T, Oh, D M, Weleber, R G, Stone, E M, Parikh, A, White, J, DeBoer-Shields, K A, Streb, L, Vallar, C

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Visual outcome following subretinal hemorrhage in Best disease von Chung, M M, Oh, K T, Streb, L M, Kimura, A E, Stone, E M

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Minna Citron's 'Feminanities': her comment on the culture of vanity von Streb, Jennifer L

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Minna Citron's "Feminanities" : her commentary on the culture of vanity von Streb, Jennifer L

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Board-level boundary scan: regaining observability with an additional IC von Ballew, W.D., Streb, L.M.

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Incoming test strategy based upon in-process failure and repair costs von Ballew, W.D., Streb, L.M.

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Linkage of Autosomal Dominant Radial Drusen (Malattia Leventinese) to Chromosome p 16–21 von Heon, E., Piguet, B., Munier, F., Sneed, S. R., Morgan, C. M., Forni, S., Pescia, G., Schorderet, D., Taylor, C. M., Streb, L. M., Wiles, C. D., Nishimura, D. Y., Sheffield, V. C., Stone, E. M.

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Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13 von Stone, E M, Nichols, B E, Streb, L M, Kimura, A E, Sheffield, V A

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Position of component testing in total quality management (TQM) von Pulat, B.M., Streb, L.M.

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APPARATUS FOR CRADLING TANKS von ERNEST L. STREB

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Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease von Stone, Edwin M., MD, PhD, Andorf, Jeaneen L., BA, Whitmore, S. Scott, PhD, DeLuca, Adam P., PhD, Giacalone, Joseph C., BS, Streb, Luan M., BA, Braun, Terry A., PhD, Mullins, Robert F., PhD, Scheetz, Todd E., PhD, Sheffield, Val C., MD, PhD, Tucker, Budd A., PhD

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