Specific transcriptional changes in human fetuses with autosomal trisomies von Altug-Teber, Ö., Bonin, M., Walter, M., Mau-Holzmann, U.A., Dufke, A., Stappert, H., Tekesin, I., Heilbronner, H., Nieselt, K., Riess, O.

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A rapid microarray based whole genome analysis for detection of uniparental disomy von Altug-Teber, Özge, Dufke, Andreas, Poths, Sven, Mau-Holzmann, Ulrike Angelika, Bastepe, Murat, Colleaux, Laurence, Cormier-Daire, Valérie, Eggermann, Thomas, Gillessen-Kaesbach, Gabriele, Bonin, Michael, Riess, Olaf

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Genotype-phenotype relationships in hepatocellular tumors from mice and man von Stahl, Sabine, Ittrich, Carina, Marx-Stoelting, Philip, Köhle, Christoph, Altug-Teber, Ozge, Riess, Olaf, Bonin, Michael, Jobst, Jürgen, Kaiser, Stephan, Buchmann, Albrecht, Schwarz, Michael

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Specific transcriptional changes in human fetuses with autosomal trisomies von Altug-Teber, Ö, Bonin, M, Walter, M, Mau-Holzmann, U A, Dufke, A, Stappert, H, Tekesin, I, Heilbronner, H, Nieselt, K, Riess, O

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Supplementary Material for: Specific transcriptional changes in human fetuses with autosomal trisomies von Altug-Teber Ö., Bonin, M., Walter, M., Mau-Holzmann, U.A., Dufke, A., Stappert, H., Tekesin, I., Heilbronner, H., Nieselt, K., Riess, O.

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Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation von Altug Teber, Özge, Gillessen-Kaesbach, Gabriele, Fischer, Sven, Böhringer, Stefan, Albrecht, Beate, Albert, Angelika, Arslan-Kirchner, Mine, Haan, Eric, Hagedorn-Greiwe, Monika, Hammans, Christof, Henn, Wolfram, Hinkel, Georg Klaus, König, Rainer, Kunstmann, Erdmute, Kunze, Jürgen, Neumann, Luitgard M, Prott, Eva-Christina, Rauch, Anita, Rott, Hans-Dieter, Seidel, Heide, Spranger, Stephanie, Sprengel, Martin, Zoll, Barbara, Lohmann, Dietmar R, Wieczorek, Dagmar

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Two brothers with Burn-McKeown syndrome von Wieczorek, Dagmar, Teber, Özge Altug, Lohmann, Dietmar, Gillessen-Kaesbach, Gabriele

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