Homozygous and heterozygous Arg614Cys mutations (1840C→T) in the ryanodine receptor gene co-segregate with malignant hyperthermia susceptibility in a German family von Rueffert, H., Olthoff, D., Deutrich, C., Thamm, B., Froster, U.G.

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Instability in the normal CTG repeat range at the myotonic dystrophy locus von Meiner, A, Thamm, B, Strenge, S, Froster, U

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Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population von Meindl, A

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The p53 status in juvenile chronic arthritis and rheumatoid arthritis von Taubert, H., Thamm, B., Meye, A., Bartel, F., Rost, A.‐K., Heidenreich, D., John, V., Brandt, J., Bache, M., Würl, P., Schmidt, H., Riemann, D.

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ABSENCE OF Yq MICRODELETIONS IN INFERTILE MEN von Tzschach, A., Thamm, B., Imthurn, B., Weber, W., Alexander, H., Glander, H.-J., Froster, U.

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Cystic fibrosis: a cause of reduced birth weight? von Müller, A E, Thamm, B, Lietz, T, Handrick, W, Walter, S

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Studies of failure mechanisms and design methods for geotextile-reinforced soil walls von Krieger, J., Thamm, B.R.

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Späte Diagnose einer myotonen Dystrophie Curschmann-Steinert bei einer Patientin mit Dilatativer Kardiomyopathie und ihrem Sohn von Gunkel, O, Reichenbach, H, Thamm, B, Wetzel, U, Bratanow, S, Kirchhof, M, Lauer, B, Froster, U, Schuler, G

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Reduced expression of hMSH2 protein is correlated to poor survival for soft tissue sarcoma patients von Taubert, Helge W., Bartel, Frank, Kappler, Matthias, Schuster, Katja, Meye, Axel, Lautenschläger, Christine, Thamm‐Mücke, Barbara, Bache, Matthias, Schmidt, Hannelore, Holzhausen, Hans‐Jürgen, Würl, Peter

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Macrocephalic mental retardation associated with a novel C-terminal MECP2 frameshift deletion von Oexle, Konrad, Thamm-Mücke, Barbara, Mayer, Thomas, Tinschert, Sigrid

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Molecular and immunohistochemical p53 status in liposarcoma and malignant fibrous histiocytoma. Identification of seven new mutations for soft tissue sarcomas von Taubert, Helge, Würl, Peter, Meye, Axel, Berger, Dieter, Thamm, Barbara, Neumann, Karsten, Hinze, Raoul, Schmidt, Hannelore, Rath, Friedrich‐Wilhelm

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De re publica ac magistratibus Megarensium ... quam ... scripsit Melchior Thamm von Thamm, Melchior, b. 1860

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Use of the phage display technique for detection of epitopes recognized by polyclonal rabbit gliadin antibodies von Osman, Awad A, Uhlig, Holm, Thamm, Barbara, Schneider-Mergener, Jens, Mothes, Thomas

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Homozygous and heterozygous Arg614Cys mutations (1840-->T) in the ryanodyne receptor gene co-segregate with malignant hyperthermia susceptibility in a German family von Rueffert, H, Olthoff, D, Deutrich, C, Thamm, B, Froster, U G

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THROMBIN GENERATION AND THE TYPE OF ANTITHROMBIN DEFICIENCY von Siegemund, A., Scholz, U., Thamm-Mücke, B., Wittig, I., Joel, A., Wittig, K., Rühlmann, C., Siegemund, T.

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Reply to “Should a syndrome be called by its correct name? The example of the preserved speech variant of Rett syndrome” by Zappella et al von Oexle, Konrad, Thamm-Mücke, Barbara, Mayer, Thomas, Tinschert, Sigrid

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P-020 Analysis of cystic fibrosis transmembrane regulator (CFTR) gene mutations in men with congenital agenesis of vas deferens von Thamm, B, Strenge, S, Reichenbach, H, Wand, D, Froster, U.G

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Problems in detecting mosaic DNA methylation in Angelman syndrome von HORSTHEMKE, Bernhard, LICH, Christina, JANSSEN, Bart, KLEINLE, Stephanie, KOCHHAN, Lothar, KRASEMANN, Ernst, KRAUS, Cornelia, KROISEL, Peter, PLENDL, Hansjörg, PURMANN, Sabine, SANDER, Gabriele, SKLADNY, Heyko, BUITING, Karin, SPITZER, Eva, THAMM-MÜCKE, Barbara, VARON-MATEEVA, Raymonda, WEINHÄUSEL, Andreas, WEIRICH, Helga, ACHMANN, Roland, AULEHLA-SCHOLZ, Christa, BAUMER, Alessandra, BÜRGER, Joachim, DWORNICZAK, Bernd, GLÄSER, Dieter, HOLINSKI-FEDER, Elke

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Pitfalls in prenatal diagnosis of DMD due to placental mosaicism of the X-chromosomes: prenatal and postnatal findings in a fetus with a deletion of exons 67-71 of the dystrophin g... von Vondran, Sigrid, Edelmann, Jeanett, Holland, Heidrun, Wolf, Claudia, Strenge, Sibylle, Thamm, Barbara, Thiele, Hannelore, Froster, Ursula G.

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Nachweis einer homozygoten C1840-T-Mutation im RYR1-Gen und Ableitung der MH-Prädisposition bei Verwandten 1. Grades von Rüffert, H., Olthoff, D., Deutrich, C., Thamm, B., Froster, U.

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