Nanoparticle-coated micro-optofluidic ring resonator as a detector for microscale gas chromatographic vapor analysis von Scholten, K, Collin, W. R, Fan, X, Zellers, E. T

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A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4 von KALAY, E, CAYLAN, R, KREMER, H, KIROGLU, A. F, YASAR, T, COLLIN, R. W. J, HEISTER, J. G. A. M, OOSTRIK, J, CREMERS, C. W. R. J, BRUNNER, H. G, KARAGUZEL, A

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Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1–2q23.3 von van Beelen, E., Schraders, M., Huygen, P.L.M., Oostrik, J., Plantinga, R.F., van Drunen, W., Collin, R.W.J., Kooper, D.P., Pennings, R.J.E., Cremers, C.W.R.J., Kremer, H., Kunst, H.P.M.

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Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan von Khan, MI, Ajmal, M, Micheal, S, Azam, M, Hussain, A, Shahzad, A, Venselaar, H, Bokhari, H, de Wijs, IJ, Hoefsloot, LH, Waheed, NK, Collin, RWJ, den Hollander, AI, Qamar, R, Cremers, FPM

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A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia von Kohl, Susanne, Coppieters, Frauke, Meire, Françoise, Schaich, Simone, Roosing, Susanne, Brennenstuhl, Christina, Bolz, Sylvia, van Genderen, Maria M., Riemslag, Frans C.C., Lukowski, Robert, den Hollander, Anneke I., Cremers, Frans P.M., De Baere, Elfride, Hoyng, Carel B., Wissinger, Bernd

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Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA : Some Evidence for Protection of the Inner Ear von DE HEER, A. R, PAUW, R. J, HUYGEN, P. L. M, COLLIN, R. W. J, KREMER, H, CREMERS, C. W. R. J

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Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA von de Heer, A.R., Pauw, R.J., Huygen, P.L.M., Collin, R.W.J., Kremer, H., Cremers, C.W.R.J.

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In Situ and Ex Situ Studies of Molybdenum Thin Films Deposited by rf and dc Magnetron Sputtering as a Back Contact for CIGS Solar Cells von Aryal, K., Khatri, H., Collins, R. W., Marsillac, S.

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Genomic approaches for the discovery of genes mutated in inherited retinal degeneration von Siemiatkowska, Anna M, Collin, Rob W J, den Hollander, Anneke I, Cremers, Frans P M

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Properties of Cu(In,Ga)Se2 Thin Films and Solar Cells Deposited by Hybrid Process von Marsillac, S., Khatri, H., Aryal, K., Collins, R. W.

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ENVIRONMENTAL JUSTICE IN OREGON: IT'S THE LAW von Collin, Robert W.

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Environmental Racism: A Challenge to Community Development von Collin, Robert W., Beatley, Timothy, Harris, William

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OR11-002 - Mutations in MVK cause non-syndromic RP von Siemiatkowska, AM, Stoffels, M, Neveling, K, Simon, A, van Hagen, PM, den Hollander, AI, Cremers, FP, van den Born, LI, Collin, RW

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Identification and expression of the first nonmammalian amyloid‐β precursor‐like protein APLP2 in the amphibian Xenopus laevis von Collin, Rob W. J., van Strien, Denise, Leunissen, Jack A. M., Martens, Gerard J. M.

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Calibration-Free Multichannel Ellipsometry for Retardance Measurement von 안일신, 오혜근, J. . Kyung(HANYANG, K. Y. Bang(HANYANG, 김옥경, R. W. Collin

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Randomized Evaluation of the Effects of Anacetrapib through Lipid-modification (REVEAL) – A large-scale, randomized, placebo-controlled trial of the clinical effects of anacetrapib... von Landray, Martin J

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Alfentanil supplemented anaesthesia for short procedures. A double-blind study of alfentanil used with etomidate and enflurane for day cases von COLLIN, R. I. W, DRUMMOND, G. B, SPENCE, A. A

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Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan von Khan, M I, Ajmal, M, Micheal, S, Azam, M, Hussain, A, Shahzad, A, Venselaar, H, Bokhari, H, de Wijs, I J, Hoefsloot, L H, Waheed, N K, Collin, R W J, den Hollander, A I, Qamar, R, Cremers, F P M

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GRAECUM LEXICON MANUALE von Benjamin Hederich, nlk20010102893

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Homelessness: The Policy and the Law von Collin, Robert W.

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