Congenital Deficiency of Vitamin K Dependent Coagulation Factors in Two Families Presents as a Genetic Defect of the Vitamin K-Epoxide-Reductase-Complex von Oldenburg, J., von Brederlow, B., Fregin, A., Rost, S., Wolz, W., Eberl, W., Eber, S., Lenz, E., Schwaab, R., Brackmann, H. H., Effenberger, W., Harbrecht, U., Schurgers, L. J., Vermeer, C., Müller, C. R.

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The Human Gene for Alkaptonuria (AKU) Maps to Chromosome 3q von Janocha, S., Wolz, W., Srsen, S., Srsnova, K., Montagutelli, X., Guénet, J.-L., Grimm, T., Kress, W., Müller, C.R.

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Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K–dependent clotting factors to the centromeric region of chromosome 16 von Fregin, Andreas, Rost, Simone, Wolz, Werner, Krebsova, Alice, Muller, Clemens R., Oldenburg, Johannes

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Genomic Sequence and Organization of the Human Gene for Cytochrome c Oxidase Subunit (COX7A1) VIIa-M von Wolz, Werner, Kress, Wolfram, Mueller, Clemens R.

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Identification of Novel Mutations in the Ryanodine-Receptor Gene (RYR1) in Malignant Hyperthermia: Genotype-Phenotype Correlation von Manning, Bernadette M., Quane, Kathleen A., Ording, Helle, Urwyler, Albert, Tegazzin, Vincenzo, Lehane, Mary, O'Halloran, John, Hartung, Edmund, Giblin, Linda M., Lynch, Patrick J., Vaughan, Pat, Censier, Kathrin, Bendixen, Diana, Comi, Giacomo, Heytens, Luc, Monsieurs, Koen, Fagerlund, Tore, Wolz, Werner, Heffron, James J.A., Muller, Clemens R., McCarthy, Tommie V.

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LayDis — an advanced navigation system for electron beam probing von Kuntzsch, C., Goldbach, M., Wolz, W.

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A Genome Wide Search for Susceptibility Loci in Three European Malignant Hyperthermia Pedigrees von Robinson, Rachel L., Monnier, Nicole, Wolz, Werner, Jung, Martin, Reis, André, Nuernberg, Gudrun, Curran, Julie L., Monsieurs, Koen, Stieglitz, Paul, Heytens, Luc, Fricker, Ruth, van Broeckhoven, Christine, Deufel, Thomas, Hopkins, Phil M., Lunardi, Joel, Mueller, Clemens R.

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Denial of visual perception von Hartmann, Joel A., Wolz, William A., Roeltgen, David P., Loverso, Felice L.

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Development of test programs in a virtual test environment von Miegler, M., Wolz, W.

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An optimized electron beam deflection assembly von Helmreich, K., Wolz, W., Batinić, M.

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Towards higher quality of design and test - perspectives of EBT tool integration von Müller-Glaser, K.D., Wolz, W.

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Reliable EBT fine positioning using correlation-based window adjustment von Scharf, R., Wolz, W., Müller-Glaser, K.D., Seitzer, D.

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Investigations on chip-internal current contrast imaging and measurement using an electron beam tester von Helmreich, K., Nagel, P., Wolz, W., Müller-Glaser, K.D.

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Sex Roles and Alcohol Consumption: A Research Note von Parker, Douglas A., Wolz, Michael W., Parker, Elizabeth S., Harford, Thomas C.

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New mutations in the ataxia telangiectasia gene von Baumer, A, Bernthaler, U, Wolz, W, Hoehn, H, Schindler, D

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Novel mutations at a CpG dinucleotide in the ryanodine receptor in malignant hyperthermia von Manning, Bernadette M., Quane, Kathleen A., Lynch, Patrick J., Urwyler, Albert, Tegazzin, Vincenzo, Krivosic-Horber, Renee, Censier, Kathrin, Comi, Giacomo, Adnet, Pascal, Wolz, Werner, Lunardi, Joel, Muller, Clemens R., McCarthy, Tommie V.

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Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter von Weber, B H, Vogt, G, Wolz, W, Ives, E J, Ewing, C C

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AN APPROACH TO CHIP-INTERNAL CURRENT MONITORING AND MEASUREMENT USING AN ELECTRON BEAM TESTER von Helmreich, K., Nagel, P., Wolz, W., Muller-Glaser, K.D.

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New mutations in tha ataxia telangiectasia gene von BAUMER, A, BERNTHALER, U, WOLZ, W, HOEHN, H, SCHINDLER, D

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Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter von Weber, Bernhard H.F, Vogt, Gudrun, Wolz, Werner, Ives, Elizabeth J, Ewing, Cecil C

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