Synpolydactyly: clinical and molecular advances von Malik, S, Grzeschik, K-H

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Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome von Doll, A., Grzeschik, K.-H.

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Point Mutations in Human GLI3 Cause Greig Syndrome von Wild, Anja, Kalff-Suske, Martha, Vortkamp, Andrea, Bornholdt, Dorothea, Kônig, Rainer, Grzeschik, Karl-Heinz

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The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia von Koch, Manuela C., Steinmeyer, Klaus, Lorenz, Claudius, Ricker, Kenneth, Wolf, Friedrich, Otto, Michael, Zoll, Barbara, Lehmann-Horn, Frank, Grzeschik, Karl-Heinz, Jentsch, Thomas J.

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Clinical variation in X-linked dominant chondrodysplasia punctata (X-linked dominant ichthyosis) von Feldmeyer, L., Mevorah, B., Grzeschik, K.H., Huber, M., Hohl, D.

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Point Mutations Throughout the GLI3 Gene Cause Greig Cephalopolysyndactyly Syndrome von Kalff-Suske, Martha, Wild, Anja, Topp, Juliane, Wessling, Martina, Jacobsen, Eva-Maria, Bornholdt, Dorothea, Engel, Hartmut, Heuer, Heike, Aalfs, Cora M., Ausems, Margreet G. E. M., Barone, Rita, Herzog, Andreas, Heutink, Peter, Homfray, Tessa, Gillessen-Kaesbach, Gabriele, König, Rainer, Kunze, Jürgen, Meinecke, Peter, Müller, Dietmar, Rizzo, Renata, Strenge, Sibylle, Superti-Furga, Andrea, Grzeschik, Karl-Heinz

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Mutational spectrum of NSDHL in CHILD syndrome von Bornholdt, D, König, A, Happle, R, Leveleki, L, Bittar, M, Danarti, R, Vahlquist, A, Tilgen, W, Reinhold, U, Poiares Baptista, A, Grosshans, É, Vabres, P, Niiyama, S, Sasaoka, K, Tanaka, T, Meiss, A L, Treadwell, P A, Lambert, D, Camacho, F, Grzeschik, K-H

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GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families von Vortkamp, Andrea, Gessler, Manfred, Grzeschik, Karl-Heinz

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The Phenotypic Spectrum of GLI3 Morphopathies Includes Autosomal Dominant Preaxial Polydactyly Type-IV and Postaxial Polydactyly Type-A/B; No Phenotype Prediction from the Position... von Radhakrishna, Uppala, Bornholdt, Dorothea, Scott, Hamish S., Patel, Uday C., Rossier, Colette, Engel, Hartmut, Bottani, Armand, Chandal, Divya, Blouin, Jean-Louis, Solanki, Jitendra V., Grzeschik, Karl-Heinz, Antonarakis, Stylianos E.

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Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts von ROEWER, L, ARNEMANN, J, SPURR, N. K, GRZESCHIK, K.-H, EPPLEN, J. T

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Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations von Debeer, Philippe, Peeters, H., Driess, S., De Smet, L., Freese, K., Matthijs, G., Bornholdt, D., Devriendt, K., Grzeschik, K.-H., Fryns, J.-P., Kalff-Suske, M.

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Genetic heterogeneity of synpolydactyly: a novel locus SPD3 maps to chromosome 14q11.2-q12 von Malik, S, Abbasi, AA, Ansar, M, Ahmad, W, Koch, MC, Grzeschik, K-H

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Mild phenotypic expression of CHILD syndrome in two generations von Alexandroff, A.B., Kinning, E., Bamford, M., Grzeschik, K.H., Milligan, A., Camp, R.D.R.

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CHILD Syndrome Caused by a Deletion of Exons 6–8 of the NSDHL Gene von Kim, C.A., König, A., Bertola, D.R., Albano, L.M.J., Gattás, G.J.F., Bornholdt, D., Leveleki, L., Happle, R., Grzeschik, K.-H.

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Differential expression of myogenic determination genes in muscle cells: possible autoactivation by the Myf gene products von Braun, T., Bober, E., Buschhausen‐Denker, G., Kohtz, S., Grzeschik, K.H., Arnold, H.H., Kotz, S.

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CHILD syndrome: the NSDHL gene and its role in CHILD syndrome, a rare hereditary disorder von Avgerinou, GP, Asvesti, AP, Katsambas, AD, Nikolaou, VA, Christofidou, EC, Grzeschik, KH, Happle, R

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Serotonin transporter gene-linked polymorphic region: Allele distributions in relationship to body weight and in anorexia nervosa von Hinney, A., Barth, N., Ziegler, A., Von Prittwitz, S., Hamann, A., Hennighausen, K., Pirke, K.M., Heils, A., Rosenkranz, K., Roth, H., Coners, H., Mayer, H., Herzog, W., Siegfried, A., Lehmkuhl, G., Poustka, F., Schmidt, M.H., Schäfer, H., Grzeschik, K.-H., Lesch, K.-P., Lentes, K.-U., Remschmidt, H., Hebebrand, J.

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The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor von Kang, Jie, Lemaire, Hans-Georg, Unterbeck, Axel, Salbaum, J. Michael, Masters, Colin L, Grzeschik, Karl-Heinz, Multhaup, Gerd, Beyreuther, Konrad, Müller-Hill, Benno

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Mutations in Bone Morphogenetic Protein Receptor 1B Cause Brachydactyly Type A2 von Lehmann, Katarina, Seemann, Petra, Stricker, Sigmar, Sammar, Marai, Meyer, Birgit, Süring, Katrin, Majewski, Frank, Tinschert, Sigrid, Grzeschik, Karl-Heinz, Müller, Dietmar, Knaus, Petra, Nürnberg, Peter, Mundlos, Stefan

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Selective Differential Display of RNAs containing interspersed repeats: analysis of changes in the transcription of HERV-K LTRs in germ cell tumors von Vinogradova, T, Leppik, L, Kalinina, E, Zhulidov, P, Grzeschik, K-H, Sverdlov, E

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