Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease? von Hedrich, Katja, Pramstaller, Peter P., Stübke, Katrin, Hiller, Anja, Kabakci, Kemal, Purmann, Sabine, Kasten, Meike, Scaglione, Cesa, Schwinger, Eberhard, Volkmann, Jens, Kostic, Vladimir, Vieregge, Peter, Martinelli, Paolo, Abbruzzese, Giovanni, Klein, Christine, Zühlke, Christine

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New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome von Beygo, Jasmin, Küchler, Alma, Gillessen-Kaesbach, Gabriele, Albrecht, Beate, Eckle, Jonas, Eggermann, Thomas, Gellhaus, Alexandra, Kanber, Deniz, Kordaß, Ulrike, Lüdecke, Hermann-Josef, Purmann, Sabine, Rossier, Eva, van de Nes, Johannes, van der Werf, Ilse M, Wenzel, Maren, Wieczorek, Dagmar, Horsthemke, Bernhard, Buiting, Karin

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Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprinted DLK1/GTL2 gene cluster von Buiting, Karin, Kanber, Deniz, Martín‐Subero, José I., Lieb, Wolfgang, Terhal, Paulien, Albrecht, Beate, Purmann, Sabine, Gross, Stephanie, Lich, Christina, Siebert, Reiner, Horsthemke, Bernhard, Gillessen‐Kaesbach, Gabriele

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Homozygous myotonic dystrophy: Clinical findings in two patients and review of the literature von Zühlke, Christine, Roeder, Elizabeth, Purmann, Sabine, Wieczorek, Dagmar, Curry, Cynthia, Loustalet, Cheri, Hellenbroich, Yorck, Richardt, Hans Helmut, Gillessen-Kaesbach, Gabriele

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Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia von Arolt, Volker, Lencer, Rebekka, Purmann, Sabine, Schürmann, Manfred, Müller-Myhsok, Bertram, Krecker, Katja, Schwinger, Eberhard

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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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Problems in detecting mosaic DNA methylation in Angelman syndrome: Letter von Horsthemke, Bernhard, Lich, Christina, Buiting, Karin, Achmann, Roland, Aulehla-Scholz, Christa, Baumer, Alessandra, Bürger, Joachim, Dworniczak, Bernd, Gläser, Dieter, Holinski-Feder, Elke, Janssen, Bart, Kleinle, Stephanie, Kochhan, Lothar, Krasemann, Ernst, Kraus, Cornelia, Kroisel, Peter, Plendl, Hansjörg, Purmann, Sabine, Sander, Gabriele, Skladny, Heyko, Spitzer, Eva, Thamm-Mücke, Barbara, Varon-Mateeva, Raymonda, Weinhäusel, Andreas, Weirich, Helga

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Problems in detecting mosaic DNA methylation in Angelman syndrome von Horsthemke, Bernhard, Lich, Christina, Buiting, Karin, Achmann, Roland, Aulehla-Scholz, Christa, Baumer, Alessandra, Bürger, Joachim, Dworniczak, Bernd, Gläser, Dieter, Holinski-Feder, Elke, Janssen, Bart, Kleinle, Stephanie, Kochhan, Lothar, Krasemann, Ernst, Kraus, Cornelia, Kroisel, Peter, Plendl, Hansjörg, Purmann, Sabine, Sander, Gabriele, Skladny, Heyko, Spitzer, Eva, Thamm-Mücke, Barbara, Varon-Mateeva, Raymonda, Weinhäusel, Andreas, Weirich, Helga

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Linkage Disequilibrium and Haplotype Analysis in German Friedreich Ataxia Families von Zühlke, Christine, Gehlken, Ulrike, Purmann, Sabine, Kunisch, Markus, Müller-Myhsok, Bertram, Kreuz, Friedmar, Laccone, Franco

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Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease von Arolt, Volker, Lencer, Rebekka, Nolte, Achim, Müller-Myhsok, Bertram, Purmann, Sabine, Schürmann, Manfred, Leutelt, Jutta, Pinnow, Marlene, Schwinger, Eberhard

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