The mouse Cat4 locus maps to Chromosome 8 and mutants express lens-corneal adhesion von Favor, J., Grimes, P., Neuhäuser-Klaus, A., Pretsch, W., Stambolian, D.

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Purkinje Cell Lineage and the Topographic Organization of the Cerebellar Cortex: A View from X Inactivation Mosaics von Baader, S.L., Schilling, M.L., Rosengarten, B., Pretsch, W., Teutsch, H.F., Oberdick, J., Schilling, K.

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The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney von Favor, J, Sandulache, R, Neuhäuser-Klaus, A, Pretsch, W, Chatterjee, B, Senft, E, Wurst, W, Blanquet, V, Grimes, P, Spörle, R, Schughart, K

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Characterization of Triosephosphate Isomerase Mutants With Reduced Enzyme Activity in Mus musculus von Merkle, S, Pretsch, W

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mouse Cat4 locus maps to Chromosome 8 and mutants express lens-corneal adhesion von Favor, J, Grimes, P, Neuhäuser-Klaus, A, Pretsch, W, Stambolian, D

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A precise localization of a mouse gene encoding increased phosphoglycerate mutase activity (Pgam1e1) on chromosome 19 von Pretsch, W, Favor, J

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A comparison of enzyme activity mutation frequencies in germ cells of mice (Mus musculus) and golden hamsters (Mesocricetus auratus) after exposure to 2 + 2 Gy γ-irradiation von Pretsch, Walter, Neuhäuser-Klaus, Angelika, Favor, Jack

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Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4 von Zhou, E, Grimes, P, Favor, J, Koeberlein, B, Pretsch, W, Neuhauser-Klaus, A, Sidjanin, D, Stambolian, D

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Electroretinography as a Screening Method for Mutations Causing Retinal Dysfunction in Mice von Dalke, Claudia, Loster, Jana, Fuchs, Helmut, Gailus-Durner, Valerie, Soewarto, Dian, Favor, Jack, Neuhauser-Klaus, Angelika, Pretsch, Walter, Gekeler, Florian, Shinoda, Kei, Zrenner, Eberhart, Meitinger, Thomas, de Angelis, Martin Hrabe, Graw, Jochen

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Enzyme-activity mutants in Mus musculus. I. Phenotypic description and genetic characterization of ethylnitrosourea-induced mutations von Pretsch, W

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Three Novel Pax6 Alleles in the Mouse Leading to the Same Small-Eye Phenotype Caused by Different Consequences at Target Promoters von Graw, Jochen, Loster, Jana, Puk, Oliver, Munster, Doris, Haubst, Nicole, Soewarto, Dian, Fuchs, Helmut, Meyer, Birgit, Nurnberg, Peter, Pretsch, Walter, Selby, Paul, Favor, Jack, Wolf, Eckhard, de Angelis, Martin Hrabe

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An ENU-induced mutation in Rs1h causes disruption of retinal structure and function von Jablonski, Monica M, Dalke, Claudia, Wang, XiaoFei, Lu, Lu, Manly, Kenneth F, Pretsch, Walter, Favor, Jack, Pardue, Machelle T, Rinchik, Eugene M, Williams, Robert W, Goldowitz, Daniel, Graw, Jochen

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Mutation in Intron 6 of the Hamster Mitf Gene Leads to Skipping of the Subsequent Exon and Creates a Novel Animal Model for the Human Waardenburg Syndrome Type II von Graw, Jochen, Pretsch, Walter, Loster, Jana

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A Mutation Affecting the Lactate Dehydrogenase Locus Ldh-1 in the Mouse. II. Mechanism of the LDH-A Deficiency Associated With Hemolytic Anemia von Pretsch, W, Merkle, S, Favor, J, Werner, T

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Hereditary Lactate Dehydrogenase A-Subunit Deficiency as Cause of Early Postimplantation Death of Homozygotes in Mus musculus von Merkle, S, Favor, J, Graw, J, Hornhardt, S, Pretsch, W

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Molecular analysis of four lactate dehydrogenase-A mutants in the mouse von Sandulache, R, Pretsch, W, Chatterjee, B, Gimbel, W, Graw, J, Favor, J

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Molecular analysis of two new Steel mutations in mice shows a transversion or an insertion von Graw, J, Löster, J, Neuhäuser-Klaus, A, Pretsch, W, Schmitt-John, T

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A 76-bp Deletion in the Mip Gene Causes Autosomal Dominant Cataract in Hfi Mice von Sidjanin, D.J., Parker-Wilson, Devonne M., Neuhäuser-Klaus, Angelika, Pretsch, Walter, Favor, Jack, Deen, Peter M.T., Ohtaka-Maruyama, Chiaki, Lu, Yun, Bragin, Alvina, Skach, William R., Chepelinsky, Ana B., Grimes, Patricia A., Stambolian, Dwight E.

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Moderate hypermutability of a transgenic lacZ reporter gene in Myc-dependent inflammation-induced plasma cell tumors in mice von FELIX, Klaus, POLACK, Axel, PRETSCH, Walter, JACKSON, Sharon H, FEIGENBAUM, Lionel, BORNKAMM, Georg-Wilhelm, JANZ, Siegfried

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Moderate G6PD deficiency increases mutation rates in the brain of mice von Felix, Klaus, Rockwood, Lynne D, Pretsch, Walter, Nair, Jagadeesan, Bartsch, Helmut, Bornkamm, Georg-Wilhelm, Janz, Siegfried

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