Molecular Distillation of Thermally Supersensitive Liquids von Frank, W. A, Kutsche, H. D

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Fractionation of polypropylene glycols in the molecular weight range of 1200–2400 using a novel apparatus von Frank, W. A., Kutsche, H. D.

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Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes von Kratz, C P, Franke, L, Peters, H, Kohlschmidt, N, Kazmierczak, B, Finckh, U, Bier, A, Eichhorn, B, Blank, C, Kraus, C, Kohlhase, J, Pauli, S, Wildhardt, G, Kutsche, K, Auber, B, Christmann, A, Bachmann, N, Mitter, D, Cremer, F W, Mayer, K, Daumer-Haas, C, Nevinny-Stickel-Hinzpeter, C, Oeffner, F, Schlüter, G, Gencik, M, Überlacker, B, Lissewski, C, Schanze, I, Greene, M H, Spix, C, Zenker, M

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Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K + channelopathies von Gripp, Karen W, Smithson, Sarah F, Scurr, Ingrid J, Baptista, Julia, Majumdar, Anirban, Pierre, Germaine, Williams, Maggie, Henderson, Lindsay B, Wentzensen, Ingrid M, McLaughlin, Heather, Leeuwen, Lisette, Simon, Marleen E H, van Binsbergen, Ellen, Dinulos, Mary Beth P, Kaplan, Julie D, McRae, Anne, Superti-Furga, Andrea, Good, Jean-Marc, Kutsche, Kerstin

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Disruption of Neurexin 1 Associated with Autism Spectrum Disorder von Kim, Hyung-Goo, Kishikawa, Shotaro, Higgins, Anne W., Seong, Ihn-Sik, Donovan, Diana J., Shen, Yiping, Lally, Eric, Weiss, Lauren A., Najm, Juliane, Kutsche, Kerstin, Descartes, Maria, Holt, Lynn, Braddock, Stephen, Troxell, Robin, Kaplan, Lee, Volkmar, Fred, Klin, Ami, Tsatsanis, Katherine, Harris, David J., Noens, Ilse, Pauls, David L., Daly, Mark J., MacDonald, Marcy E., Morton, Cynthia C., Quade, Bradley J., Gusella, James F.

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Phenotypic spectrum associated with CASK loss-of-function mutations von Moog, Ute, Kutsche, Kerstin, Kortüm, Fanny, Chilian, Bettina, Bierhals, Tatjana, Apeshiotis, Neophytos, Balg, Stefanie, Chassaing, Nicolas, Coubes, Christine, Das, Soma, Engels, Hartmut, Van Esch, Hilde, Grasshoff, Ute, Heise, Marisol, Isidor, Bertrand, Jarvis, Joanna, Koehler, Udo, Martin, Thomas, Oehl-Jaschkowitz, Barbara, Ortibus, Els, Pilz, Daniela T, Prabhakar, Prab, Rappold, Gudrun, Rau, Isabella, Rettenberger, Günther, Schlüter, Gregor, Scott, Richard H, Shoukier, Moonef, Wohlleber, Eva, Zirn, Birgit, Dobyns, William B, Uyanik, Gökhan

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P6376The role of circulating lymphocytes on hypertensive heart disease von Schluter, K.-D, Schreckenberg, R, Wolf, A, Kutsche, H, Troidl, C, Simsekyilmaz, S, Niemann, B

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P6372Does modification of activity regimes optimize the effect of high physical activity on hypertensive heart disease? von Schluter, K.-D, Schreckenberg, R, Wolf, A, Kutsche, H, Troidl, C, Simsekyilmaz, S, Niemann, B, Schulz, R

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Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome von Schulz, AL, Albrecht, B, Arici, C, Van Der Burgt, I, Buske, A, Gillessen-Kaesbach, G, Heller, R, Horn, D, Hübner, CA, Korenke, GC, König, R, Kress, W, Krüger, G, Meinecke, P, Mücke, J, Plecko, B, Rossier, E, Schinzel, A, Schulze, A, Seemanova, E, Seidel, H, Spranger, S, Tuysuz, B, Uhrig, S, Wieczorek, D, Kutsche, K, Zenker, M

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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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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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Refining the phenotype of α-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly von Morris-Rosendahl, DJ, Najm, J, Lachmeijer, AMA, Sztriha, L, Martins, M, Kuechler, A, Haug, V, Zeschnigk, C, Martin, P, Santos, M, Vasconcelos, C, Omran, H, Kraus, U, Van der Knaap, MS, Schuierer, G, Kutsche, K, Uyanik, G

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Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K+ channelopathies von Gripp, Karen W, Smithson, Sarah F, Scurr, Ingrid J, Baptista, Julia, Majumdar, Anirban, Pierre, Germaine, Williams, Maggie, Henderson, Lindsay B, Wentzensen, Ingrid M, McLaughlin, Heather, Leeuwen, Lisette, Simon, Marleen E H, van Binsbergen, Ellen, Dinulos, Mary Beth P, Kaplan, Julie D, McRae, Anne, Superti-Furga, Andrea, Good, Jean-Marc, Kutsche, Kerstin

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A physical map of the mouse genome von Bentley, David R, Gregory, Simon G, Sekhon, Mandeep, Schein, Jacqueline, Zhao, Shaying, Osoegawa, Kazutoyo, Scott, Carol E, Evans, Richard S, Burridge, Paul W, Cox, Tony V, Fox, Christopher A, Hutton, Richard D, Mullenger, Ian R, Phillips, Kimbly J, Smith, James, Stalker, Jim, Threadgold, Glen J, Birney, Ewan, Wylie, Kristine, Chinwalla, Asif, Wallis, John, Hillier, LaDeana, Carter, Jason, Gaige, Tony, Jaeger, Sara, Kremitzki, Colin, Layman, Dan, Maas, Jason, McGrane, Rebecca, Mead, Kelly, Walker, Rebecca, Jones, Steven, Smith, Michael, Asano, Jennifer, Bosdet, Ian, Chan, Susanna, Chittaranjan, Suganthi, Chiu, Readman, Fjell, Chris, Fuhrmann, Dan, Girn, Noreen, Gray, Catharine, Guin, Ran, Hsiao, Letticia, Krzywinski, Martin, Kutsche, Reta, Lee, Soo Sen, Mathewson, Carrie, McLeavy, Candice, Messervier, Steve, Ness, Steven, Pandoh, Pawan, Prabhu, Anna-Liisa, Saeedi, Parvaneh, Smailus, Duane, Spence, Lorraine, Stott, Jeff, Taylor, Sheryl, Terpstra, Wesley, Tsai, Miranda, Vardy, Jill, Wye, Natasja, Yang, George, Shatsman, Sofiya, Ayodeji, Bola, Geer, Keita, Tsegaye, Getahun, Shvartsbeyn, Alla, Gebregeorgis, Elizabeth, Krol, Margaret, Russell, Daniel, Overton, Larry, Malek, Joel A, Holmes, Mike, Heaney, Michael, Shetty, Jyoti, Feldblyum, Tamara, Nierman, William C, Catanese, Joseph J, Hubbard, Tim, Waterston, Robert H, Rogers, Jane, de Jong, Pieter J, Fraser, Claire M, Marra, Marco, McPherson, John D

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Mutations in ARHGEF6 , encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation von Gal, Andreas, Kutsche, Kerstin, Yntema, Helger, Brandt, Alexander, Jantke, Inka, Gerd Nothwang, Hans, Orth, Ulrike, Boavida, Maria G, David, Dezsö, Chelly, Jamel, Fryns, Jean-Pierre, Moraine, Claude, Ropers, Hans-Hilger, Hamel, Ben C.J, van Bokhoven, Hans

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Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly von Morris-Rosendahl, D J, Najm, J, Lachmeijer, A M A, Sztriha, L, Martins, M, Kuechler, A, Haug, V, Zeschnigk, C, Martin, P, Santos, M, Vasconcelos, C, Omran, H, Kraus, U, Van der Knaap, M S, Schuierer, G, Kutsche, K, Uyanik, G

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The role of the multidisciplinary health care team in the management of patients with Marfan syndrome von von Kodolitsch, Yskert, Rybczynski, Meike, Vogler, Marina, Mir, Thomas S, Schüler, Helke, Kutsche, Kerstin, Rosenberger, Georg, Detter, Christian, Bernhardt, Alexander M, Larena-Avellaneda, Axel, Kölbel, Tilo, Debus, E Sebastian, Schroeder, Malte, Linke, Stephan J, Fuisting, Bettina, Napp, Barbara, Kammal, Anna Lena, Püschel, Klaus, Bannas, Peter, Hoffmann, Boris A, Gessler, Nele, Vahle-Hinz, Eva, Kahl-Nieke, Bärbel, Thomalla, Götz, Weiler-Normann, Christina, Ohm, Gunda, Neumann, Stefan, Benninghoven, Dieter, Blankenberg, Stefan, Pyeritz, Reed E

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Isospin tracing: A probe of nonequilibrium in central heavy-Ion collisions von Rami, F, Leifels, Y, de Schauenburg B, Gobbi, A, Hong, B, Alard, JP, Andronic, A, Averbeck, R, Barret, V, V, Basrak, Z, Bastid, N, Belyaev, I, I, Bendarag, A, Berek, G, Caplar, R, Cindro, N, Crochet, P, Devismes, A, Dupieux, P, Dzelalija, M, Eskef, M, Finck, C, Fodor, Z, Folger, H, Fraysse, L, Genoux-Lubain, A

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Transition from in-plane to out-of-plane azimuthal enhancement in Au+Au collisions von Andronic, A, Stoicea, G, Petrovici, M, Simion, V, Crochet, P, Alard, J.P, Averbeck, R, Barret, V, Basrak, Z, Bastid, N, Bendarag, A, Berek, G, Čaplar, R, Devismes, A, Dupieux, P, Dželalija, M, Eskef, M, Finck, Ch, Fodor, Z, Gobbi, A, Grishkin, Y, Hartmann, O.N, Herrmann, N, Hildenbrand, K.D, Hong, B, Kecskemeti, J, Kim, Y.J, Kirejczyk, M, Korolija, M, Kotte, R, Kress, T, Kutsche, R, Lebedev, A, Lee, K.S, Leifels, Y, Manko, V, Merlitz, H, Neubert, W, Pelte, D, Plettner, C, Rami, F, Reisdorf, W, de Schauenburg, B, Schüll, D, Seres, Z, Sikora, B, Sim, K.S, Siwek-Wilczyńska, K, Smolyankin, V, Stockmeier, M.R, Vasiliev, M, Wagner, P, Wiśniewski, K, Wohlfarth, D, Yushmanov, I, Zhilin, A

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Novel mutations in BCOR in three patients with oculo-facio-cardio-dental syndrome, but none in Lenz microphthalmia syndrome von HORN, Denise, CHYREK, Magdalena, WIECZOREK, Dagmar, GILLESSEN-KAESBACH, Gabriele, KUTSCHE, Kerstin, KLEIER, Saskia, LÜTTGEN, Sabine, BOLZ, Hanno, HINKEL, Georg-Klaus, KORENKE, Georg Christoph, RIESS, Angelika, SCHELL-APACIK, Can, TINSCHERT, Sigrid

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