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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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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Spring wheel von KUTSCHE ARTHUR H

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Spring wheel von KUTSCHE ARTHUR H

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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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MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency von Knapp, Karen M, Jenkins, Danielle E, Sullivan, Rosie, Harms, Frederike L, von Elsner, Leonie, Ockeloen, Charlotte W, de Munnik, Sonja, Bongers, Ernie M H F, Murray, Jennie, Pachter, Nicholas, Denecke, Jonas, Kutsche, Kerstin, Bicknell, Louise S

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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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Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci von Chilian, B, Abdollahpour, H, Bierhals, T, Haltrich, I, Fekete, G, Nagel, I, Rosenberger, G, Kutsche, K

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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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Evaluating the quality of Marfan genotype–phenotype correlations in existing FBN1 databases von Groth, Kristian A., Von Kodolitsch, Yskert, Kutsche, Kerstin, Gaustadnes, Mette, Thorsen, Kasper, Andersen, Niels H., Gravholt, Claus H.

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Mutation of CDH23 , encoding a new member of the cadherin gene family, causes Usher syndrome type 1D von Gal, Andreas, Bolz, Hanno, von Brederlow, Benigna, Ramírez, Alfredo, Bryda, Elizabeth C, Kutsche, Kerstin, Nothwang, Hans Gerd, Seeliger, Mathias, Cabrera, Maria del C.-Salcedó, Vila, Manuel Caballeró, Molina, Orfilio Pelaez, Kubisch, Christian

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Biallelic FRA10AC1 variants cause a neurodevelopmental disorder with growth retardation von von Elsner, Leonie, Chai, Guoliang, Schneeberger, Pauline E, Harms, Frederike L, Casar, Christian, Qi, Minyue, Alawi, Malik, Abdel-Salam, Ghada M H, Zaki, Maha S, Arndt, Florian, Yang, Xiaoxu, Stanley, Valentina, Hempel, Maja, Gleeson, Joseph G, Kutsche, Kerstin

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The novel centrosomal associated protein CEP55 is present in the spindle midzone and the midbody von Martinez-Garay, Isabel, Rustom, Amin, Gerdes, Hans-Hermann, Kutsche, Kerstin

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PROCEDIMENTO PER LA PRODUZIONE DI MAGLIERIE A SPUGNA SU MACCHINE CIR COLARI PER MAGLIERIA A CADUTE MULTIPLE von KUTSCHE H, KURTH H, HORTENBACH R, DORRER K

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The Neural Recognition Molecule L1 Is a Sialic Acid-binding Lectin for CD24, Which Induces Promotion and Inhibition of Neurite Outgrowth von Kleene, Ralf, Yang, Huibin, Kutsche, Michael, Schachner, Melitta

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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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