Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations von Wehner, L-E, Folz, BJ, Argyriou, L, Twelkemeyer, S, Teske, U, Geisthoff, UW, Werner, JA, Engel, W, Nayernia, K

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Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals von Solomon, Benjamin D, Lacbawan, Felicitas, Mercier, Sandra, Clegg, Nancy J, Delgado, Mauricio R, Rosenbaum, Kenneth, Dubourg, Christèle, David, Veronique, Olney, Ann Haskins, Wehner, Lars-Erik, Hehr, Ute, Bale, Sherri, Paulussen, Aimee, Smeets, Hubert J, Hardisty, Emily, Tylki-Szymanska, Anna, Pronicka, Ewa, Clemens, Michelle, McPherson, Elizabeth, Hennekam, Raoul C M, Hahn, Jin, Stashinko, Elaine, Levey, Eric, Wieczorek, Dagmar, Roeder, Elizabeth, Schell-Apacik, Chayim Can, Booth, Carol W, Thomas, Ronald L, Kenwrick, Sue, Cummings, Derek A T, Bous, Sophia M, Keaton, Amelia, Balog, Joan Z, Hadley, Donald, Zhou, Nan, Long, Robert, Vélez, Jorge I, Pineda-Alvarez, Daniel E, Odent, Sylvie, Roessler, Erich, Muenke, Maximilian

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Herpesvirus saimiri Tip gene causes T-cell lymphomas in transgenic mice von Wehner, L E, Schröder, N, Kamino, K, Friedrich, U, Biesinger, B, Rüther, U

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Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations von Zenker, Martin, Lehmann, Katarina, Schulz, Anna Leana, Barth, Helmut, Hansmann, Dagmar, Koenig, Rainer, Korinthenberg, Rudolf, Kreiss-Nachtsheim, Martina, Meinecke, Peter, Morlot, Susanne, Mundlos, Stefan, Quante, Anne S, Raskin, Salmo, Schnabel, Dirk, Wehner, Lars-Erik, Kratz, Christian P, Horn, Denise, Kutsche, Kerstin

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Germline KRAS mutations cause Noonan syndrome von Schubbert, Suzanne, Zenker, Martin, Rowe, Sara L, Böll, Silke, Klein, Cornelia, Bollag, Gideon, van der Burgt, Ineke, Musante, Luciana, Kalscheuer, Vera, Wehner, Lars-Erik, Nguyen, Hoa, West, Brian, Zhang, Kam Y J, Sistermans, Erik, Rauch, Anita, Niemeyer, Charlotte M, Shannon, Kevin, Kratz, Christian P

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SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome von Zenker, Martin, Horn, Denise, Wieczorek, Dagmar, Allanson, Judith, Pauli, Silke, van der Burgt, Ineke, Doerr, Helmuth-Guenther, Gaspar, Harald, Hofbeck, Michael, Gillessen-Kaesbach, Gabriele, Koch, Andreas, Meinecke, Peter, Mundlos, Stefan, Nowka, Anja, Rauch, Anita, Reif, Silke, von Schnakenburg, Christian, Seidel, Heide, Wehner, Lars-Erik, Zweier, Christiane, Bauhuber, Susanne, Matejas, Verena, Kratz, Christian P, Thomas, Christoph, Kutsche, Kerstin

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CHARGE – von einer Assoziation zum Syndrom von Pauli, S., Steckel, M., Zoll, B., Wehner, L.-E.

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ALK‐1 mutations in liver transplanted patients with hereditary hemorrhagic telangiectasia von Argyriou, Loukas, Pfitzmann, Robert, Wehner, Lars‐Erik, Twelkemeyer, Stefan, Neuhaus, Peter, Nayernia, Karim, Engel, Wolfgang

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Short Report: Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations von L-E Wehner, Folz, B J, Argyriou, L, Twelkemeyer, S, Teske, U, Geisthoff, U W, Werner, JA, Engel, W, Nayernia, K

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Novel mutations in the ENG and ACVRL1 genes causing hereditary hemorrhagic teleangiectasia von Argyriou, Loukas, Twelkemeyer, Stefan, Panchulidze, Irakli, Wehner, Lars-Erik, Teske, Ute, Engel, Wolfgang, Nayernia, Karim

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Mutation analysis of the M6b gene in patients with Pelizaeus-Merzbacher-like syndrome von Henneke, Marco, Wehner, Lars-Erik, Hennies, Hans Christian, Preuß, Natalie, Gärtner, Jutta

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Mutation analysis of the M6b-gene in patients with Pelizaeus-Merzbacher-like syndrome von Henneke, M, Wehner, LE, Hennies, HC, Preuß, N, Gärtner, J

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Take-or-Pay Gas-Purchase Contracts von Wehner, E L, Voelkel, Stanley H

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THE BENEFITS OF GLOBAL HIGH RESOLUTION FOR CLIMATE SIMULATION: Process Understanding and the Enabling of Stakeholder Decisions at the Regional Scale von Roberts, M. J., Vidale, P. L., Senior, C., Hewitt, H. T., Bates, C., Berthou, S., Chang, P., Christensen, H. M., Danilov, S., Demory, M.-E., Griffies, S. M., Haarsma, R., Jung, T., Martin, G., Minobe, S., Ringler, T., Satoh, M., Schiemann, R., Scoccimarro, E., Stephens, G., Wehner, M. F.

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Contributions of Anthropogenic and Natural Forcing to Recent Tropopause Height Changes von Santer, B. D., Wehner, M. F., Wigley, T. M. L., Sausen, R., Meehl, G. A., Taylor, K. E., Ammann, C., Arblaster, J., Washington, W. M., Boyle, J. S., Brüggemann, W.

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[18F]mFBG long axial field of view PET-CT without general anaesthesia reveals concise extension of neuroblastoma in a 9-month-old boy von Borgwardt, L., Brok, J. S., Andersen, K. F., Madsen, J., Gillings, N., Fosbøl, M.Ø., Denholt, C. L., Wehner, P. S., Enevoldsen, L. H., Oturai, P., Czyzewska, D., Johannesen, H. H., Højgaard, L., Petersen, I. N., Sørensen, L. S., Schulze, C., Saxtoft, E. S., Andersen, F. L., Fischer, B. M.

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Loophole-free Bell inequality violation using electron spins separated by 1.3 kilometres von Hensen, B., Bernien, H., Dréau, A. E., Reiserer, A., Kalb, N., Blok, M. S., Ruitenberg, J., Vermeulen, R. F. L., Schouten, R. N., Abellán, C., Amaya, W., Pruneri, V., Mitchell, M. W., Markham, M., Twitchen, D. J., Elkouss, D., Wehner, S., Taminiau, T. H., Hanson, R.

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Separating signal and noise in atmospheric temperature changes: The importance of timescale von Santer, B. D., Mears, C., Doutriaux, C., Caldwell, P., Gleckler, P. J., Wigley, T. M. L., Solomon, S., Gillett, N. P., Ivanova, D., Karl, T. R., Lanzante, J. R., Meehl, G. A., Stott, P. A., Taylor, K. E., Thorne, P. W., Wehner, M. F., Wentz, F. J.

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Timeliness of Early Childhood Vaccinations and Undervaccination Patterns in Montana von Newcomer, Sophia R., Freeman, Rain E., Wehner, Bekki K., Anderson, Stacey L., Daley, Matthew F.

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Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR Activity von Hornig, N. C, Ukat, M, Schweikert, H. U, Hiort, O, Werner, R, Drop, S. L. S, Cools, M, Hughes, I. A, Audi, L, Ahmed, S. F, Demiri, J, Rodens, P, Worch, L, Wehner, G, Kulle, A. E, Dunstheimer, D, Müller-Roßberg, E, Reinehr, T, Hadidi, A. T, Eckstein, A. K, van der Horst, C, Seif, C, Siebert, R, Ammerpohl, O, Holterhus, P.-M

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