Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism von Bramswig, Nuria C., Lüdecke, H.-J., Pettersson, M., Albrecht, B., Bernier, R. A., Cremer, K., Eichler, E. E., Falkenstein, D., Gerdts, J., Jansen, S., Kuechler, A., Kvarnung, M., Lindstrand, A., Nilsson, D., Nordgren, A., Pfundt, R., Spruijt, L., Surowy, H. M., de Vries, B. B. A., Wieland, T., Engels, H., Strom, T. M., Kleefstra, T., Wieczorek, D.

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‘Splitting versus lumping’: Temple–Baraitser and Zimmermann–Laband Syndromes von Bramswig, Nuria C., Ockeloen, C. W., Czeschik, J. C., van Essen, A. J., Pfundt, R., Smeitink, J., Poll-The, B. T., Engels, H., Strom, T. M., Wieczorek, D., Kleefstra, T., Lüdecke, H.-J.

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Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype von Bramswig, Nuria C., Caluseriu, O., Lüdecke, H.-J., Bolduc, F. V., Noel, N. C. L., Wieland, T., Surowy, H. M., Christen, H.-J., Engels, H., Strom, T. M., Wieczorek, D.

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Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome von Czeschik, J. C., Voigt, C., Alanay, Y., Albrecht, B., Avci, S., FitzPatrick, D., Goudie, D. R., Hehr, U., Hoogeboom, A. J., Kayserili, H., Simsek-Kiper, P. O., Klein-Hitpass, L., Kuechler, A., López-González, V., Martin, M., Rahmann, S., Schweiger, B., Splitt, M., Wollnik, B., Lüdecke, H. -J., Zeschnigk, M., Wieczorek, D.

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Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses von Wuyts, Wim, Van Hul, Wim, De Boulle, Kristel, Hendrickx, Jan, Bakker, Egbert, Vanhoenacker, Filip, Mollica, Florindo, Lüdecke, Hermann-Josef, Sayli, Bekir Sitki, Pazzaglia, Ugo E., Mortier, Geert, Hamel, Ben, Conrad, Ernest U., Matsushita, Mark, Raskind, Wendy H., Willems, Patrick J.

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A NECTAr-based upgrade for the Cherenkov cameras of the H.E.S.S. 12-meter telescopes von Ashton, T., Backes, M., Balzer, A., Berge, D., Bolmont, J., Bonnefoy, S., Brun, F., Chaminade, T., Delagnes, E., Fontaine, G., Füßling, M., Giavitto, G., Giebels, B., Glicenstein, J.-F., Gräber, T., Hinton, J.A., Jahnke, A., Klepser, S., Kossatz, M., Kretzschmann, A., Lefranc, V., Leich, H., Lenain, J.-P., Lüdecke, H., Lypova, I., Manigot, P., Marandon, V., Moulin, E., Murach, T., de Naurois, M., Nayman, P., Ohm, S., Penno, M., Ross, D., Salek, D., Schade, M., Schwab, T., Shiningayamwe, K., Stegmann, C., Steppa, C., Tavernet, J.-P., Thornhill, J., Toussenel, F., Vincent, P.

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Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I von Glöckner, Gernot, Momeni, Parastoo, Albrecht, Beate, Lüdecke, Hermann-Josef, Zabel, Bernhard, Gillessen-Kaesbach, Gabriele, Schmidt, Olaf, Meinecke, Peter, Rosenthal, André, Hennekam, Raoul, von Holtum, Diane, Horsthemke, Bernhard

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Multi-periodic climate dynamics: spectral analysis of long-term instrumental and proxy temperature records von Lüdecke, H.-J, Hempelmann, A, Weiss, C. O

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Pronounced short stature in a girl with tricho‐rhino‐phalangeal syndrome II (TRPS II, Langer–Giedion syndrome) and growth hormone deficiency von Riedl, S., Giedion, A., Schweitzer, K., Müllner‐Eidenböck, A., Grill, F., Frisch, H., Lüdecke, H.‐J.

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Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer—Giedion syndrome von Lüdecke, Hermann-Josef, J.Wagner, Michael, Nardmann, Judith, Pillo, Biagio La, E.Parrish, Julia, J.Willems, Patrick, A.Haan, Eric, Frydman, Moshe, J.H.Hamers, Guus, E.Weils, Dan, Horsthemke, Bernhard

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Tricho-Rhino-Phalangeal Syndrome with Supernumerary Teeth von Kantaputra, P., Miletich, I., Lüdecke, H.-J., Suzuki, E.Y., Praphanphoj, V., Shivdasani, R., Wuelling, M., Vortkamp, A., Napierala, D., Sharpe, P.T.

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Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III von Lüdecke, H.-J., Schaper, J., Meinecke, P., Momeni, P., Groß, S., von Holtum, D., Hirche, H., Abramowicz, M.J., Albrecht, B., Apacik, C., Christen, H.-J., Claussen, U., Devriendt, K., Fastnacht, E., Forderer, A., Friedrich, U., Goodship, T.H.J., Greiwe, M., Hamm, H., Hennekam, R.C.M., Hinkel, G.K., Hoeltzenbein, M., Kayserili, H., Majewski, F., Mathieu, M., McLeod, R., Midro, A.T., Moog, U., Nagai, T., Niikawa, N., Ørstavik, K.H., Plöchl, E., Seitz, C., Schmidtke, J., Tranebjærg, L., Tsukahara, M., Wittwer, B., Zabel, B., Gillessen-Kaesbach, G., Horsthemke, B.

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Detailed characterization of electron sources yielding first demonstration of European X-ray Free-Electron Laser beam quality von Stephan, F., Boulware, C. H., Krasilnikov, M., Bähr, J., Asova, G., Donat, A., Gensch, U., Grabosch, H. J., Hänel, M., Hakobyan, L., Henschel, H., Ivanisenko, Y., Jachmann, L., Khodyachykh, S., Khojoyan, M., Köhler, W., Korepanov, S., Koss, G., Kretzschmann, A., Leich, H., Lüdecke, H., Meissner, A., Oppelt, A., Petrosyan, B., Pohl, M., Riemann, S., Rimjaem, S., Sachwitz, M., Schöneich, B., Scholz, T., Schulze, H., Schultze, J., Schwendicke, U., Shapovalov, A., Spesyvtsev, R., Staykov, L., Tonisch, F., Walter, T., Weisse, S., Wenndorff, R., Winde, M., Vu, L. v., Dürr, H., Kamps, T., Richter, D., Sperling, M., Ovsyannikov, R., Vollmer, A., Knobloch, J., Jaeschke, E., Boster, J., Brinkmann, R., Choroba, S., Flechsenhar, K., Flöttmann, K., Gerdau, W., Katalev, V., Koprek, W., Lederer, S., Martens, C., Pucyk, P., Schreiber, S., Simrock, S., Vogel, E., Vogel, V., Rosbach, K., Bonev, I., Tsakov, I., Michelato, P., Monaco, L., Pagani, C., Sertore, D., Garvey, T., Will, I., Templin, I., Sandner, W., Ackermann, W., Arévalo, E., Gjonaj, E., Müller, W. F. O., Schnepp, S., Weiland, T., Wolfheimer, F., Rönsch, J., Rossbach, J.

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First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome von Beygo, J., Buiting, K., Seland, S., Lüdecke, H.-J., Hehr, U., Lich, C., Prager, B., Lohmann, D.R., Wieczorek, D.

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DYT16 mimics metabolic disease with fever associated beginning of dystonia and MRI abnormalities von Kölbel, H, Kuechler, A, Strom, T.M, Lüdecke, H.-J, Möller-Hartmann, C, Della-Marina, A, Wieczoreck, D, Schara, U

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High temperature wear testing of a Ni-based superalloy pin on a cast iron disc von Rynio, C., Hattendorf, H., Klöwer, J., Lüdecke, H.-G., Eggeler, G.

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A Novel Homozygous WDR72 Mutation in Two Siblings with Amelogenesis Imperfecta and Mild Short Stature von Kuechler, A., Hentschel, J., Kurth, I., Stephan, B., Prott, E.-C., Schweiger, B., Schuster, A., Wieczorek, D., Lüdecke, H.-J.

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Cloning of the putative tumour suppressor gene for hereditary multiple exostoses ( EXT1 ) von Ahn, Jung, Lüdecke, Hermann-Josef, Lindow, Steffi, Horton, William A, Lee, Brendan, Wagner, Michael J, Horsthemke, Bernhard, Wells, Dan E

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High temperature wear testing of a Ni-based superalloy pin on a cast iron disc; Hochtemperatur-Verschleißversuche am Tribosystem Alloy 80A - Gusseisen mittels Stift-auf-Scheibe Ano... von Rynio, C, Hattendorf, H, Klower, J, Ludecke, H-G, Eggeler, G

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Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification von Lüdecke, Hermann-Josef, Senger, Gabriele, Claussen, Uwe, Horsthemke, Bernhard

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