Focused Fluid Flow Along the Nootka Fault Zone and Continental Slope, Explorer‐Juan de Fuca Plate Boundary von Riedel, M., Rohr, K. M. M., Spence, G. D., Kelley, D., Delaney, J., Lapham, L., Pohlman, J. W., Hyndman, R. D., Willoughby, E. C.

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Mutational screening of VSX1 in keratoconus patients from the European population von Dash, D P, George, S, O'Prey, D, Burns, D, Nabili, S, Donnelly, U, Hughes, A E, Silvestri, G, Jackson, J, Frazer, D, Héon, E, Willoughby, C E

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Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia von Guazzarotti, L., Tadini, G., Mancini, G.E., Giglio, S., Willoughby, C.E., Callea, M., Sani, I., Nannini, P., Mameli, C., Tenconi, A.A., Mauri, S., Bottero, A., Caimi, A., Morelli, M., Zuccotti, G.V.

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A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathy von Chamney, S, McLoone, E, Willoughby, C E

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Collagen Corneal Shields von Willoughby, C.E, Batterbury, M, Kaye, S.B

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Seafloor compliance imaging of marine gas hydrate deposits and cold vent structures von Willoughby, E. C., Latychev, K., Edwards, R. N., Schwalenberg, K., Hyndman, R. D.

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Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43) von Musa, F U, Ratajczak, P, Sahu, J, Pentlicky, S, Fryer, A, Richard, G, Willoughby, C E

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A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract von Willoughby, C E, Arab, Sara, Gandhi, R, Zeinali, S, Arab, Seddigheh, Luk, D, Billingsley, G, Munier, F L, Héon, E

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Osmotic tolerance limits and properties of murine spermatozoa von Willoughby, C.E. (Methodist Hospital of Indiana Inc., Indianapolis, IN.), Mazur, P, Peter, A.T, Critser, J.K

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The ocular phenotype of stiff-skin syndrome von Chamney, S, Cartmill, B, Earley, O, McConnell, V, Willoughby, C E

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Epstein-Barr virus (types 1 and 2) in the tear film in Sjogren's syndrome and HIV infection von Willoughby, C.E., Baker, K., Kaye, S.B., Carey, P., O'Donnell, N., Field, A., Longman, L., Bucknall, R., Hart, C.A.

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A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family von Callea, M., Nieminen, P., Willoughby, C.E., Clarich, G., Yavuz, I., Vinciguerra, A., Di Stazio, M., Giglio, S., Sani, I., Maglione, M., Pensiero, S., Tadini, G., Bellacchio, E.

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Effects of Percoll separation, cryoprotective agents, and temperature on plasma membrane permeability characteristics of murine spermatozoa and their relevance to cryopreservation von Phelps, M.J, Liu, J, Benson, J.D, Willoughby, C.E, Gilmore, J.A, Critser, J.K

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Identification of a novel frameshift mutation in the EDAR gene causing autosomal dominant hypohidrotic ectodermal dysplasia von Callea, M., Willoughby, C.E., Nieminen, P., Di Stazio, M., Bellacchio, E., Giglio, S., Sani, I., Vinciguerra, A., Maglione, M., Tadini, G., Clarich, G.

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Earthquake rate, slip rate, and the effective seismic thickness for oceanic transform faults of the Juan de Fuca plate system von Willoughby, E. C., Hyndman, R. D.

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Shear velocities in Cascadia from seafloor compliance measurements von Willoughby, E. C., Edwards, R. N.

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Oral manifestations in a boy with X-linked reticulate pigmentary disorder von Callea, M, Maglione, M, Yavuz, I, Deroma, L, Willoughby, CE, Tadini, G

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Temporal fluctuations of microseismic noise in Yellowstone's Upper Geyser Basin from a continuous gravity observation von Tikku, A. A., McAdoo, D. C., Schenewerk, M. S., Willoughby, E. C.

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The preparation of laminated ceramic composites using paint technology von WILLOUGHBY, C. E. P, EVANS, J. R. G

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Molecular diagnosis for heterogeneous genetic diseases with targeted high-throughput DNA sequencing applied to retinitis pigmentosa von Simpson, David A, Clark, Graeme R, Alexander, Sharon, Silvestri, Giuliana, Willoughby, Colin E

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