Severe forms of Baraitser-Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations von Di Donato, N, Rump, A, Koenig, R, Der Kaloustian, V M, Halal, F, Sonntag, K, Krause, C, Hackmann, K, Hahn, G, Schrock, E, Verloes, A

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PUF60-SCRIB fusion transcript in a patient with 8q24.3 microdeletion and atypical Verheij syndrome von Abdin, D., Rump, A., Tzschach, A., Sarnow, K., Schröck, E., Hackmann, K., Di Donato, N.

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Severe forms of Baraitser–Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations von Di Donato, N, Rump, A, Koenig, R, Der Kaloustian, V M, Halal, F, Sonntag, K, Krause, C, Hackmann, K, Hahn, G, Schrock, E, Verloes, A

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Distinct phenotype of PHF6 deletions in females von Di Donato, N, Isidor, B, Lopez Cazaux, S, Le Caignec, C, Klink, B, Kraus, C, Schrock, E, Hackmann, K

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Expanding the clinical and neuroradiological phenotype of 6q27 microdeletion: Olfactory bulb aplasia and anosmia von Gerber, J.C., Neuhann, T.M., Tyshchenko, N., Smitka, M., Hackmann, K.

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Interstitial deletion 1p36.32 in two brothers with a distinct phenotype – Overgrowth, macrocephaly and nearly normal intellectual function von Di Donato, N, Klink, B, Hahn, G, Schrock, E, Hackmann, K

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A further patient with van Maldergem syndrome von Neuhann, T.M, Müller, D, Hackmann, K, Holzinger, S, Schrock, E, Di Donato, N

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Macrocephaly, obesity, mental (intellectual) disability, and ocular abnormalities: Alternative definition and further delineation of MOMO syndrome von Di Donato, N., Riess, A., Hackmann, K., Rump, A., Huebner, A., von der Hagen, M., Hahn, G., Schrock, E., Tinschert, S.

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A new autosomal dominant syndrome of distinctive face showing ptosis and prominent eyes associated with cleft palate, ear anomalies, and learning disability von Tyshchenko, N., Neuhann, T.M., Gerlach, E., Hahn, G., Heisch, K., Rump, A., Schrock, E., Tinschert, S., Hackmann, K.

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P.2.c.041 Biomarkers for the combined efficacy of cognitive behavioural therapy in antidepressant treatment in depression von Nocon, A, Hackmann, K, Pfister, H, Heldmann, B, Rosenhagen, M, Lucae, S, Ising, M

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Selection of a highly invasive neuroblastoma cell population through long-term human cytomegalovirus infection von Michaelis, M, Barth, S, Breitling, R, Bruch, J, Steinberger, D, Rothweiler, F, Hackmann, K, Schröck, E, Doerr, H W, Griffin, D K, Cinatl, J, Cinatl, J

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Clonal Evolution Including Partial Loss of Human Leukocyte Antigen Genes Favoring Extramedullary Acute Myeloid Leukemia Relapse After Matched Related Allogeneic Hematopoietic Stem... von STÖLZEL, Friedrich, HACKMANN, Karl, ILLMER, Thomas, SCHAICH, Markus, SELIGER, Barbara, HARTMANN, Arndt, BARETTON, Gustavo, ZIETZ, Christian, EHNINGER, Gerhard, SCHROCK, Evelin, BORNHÄUSER, Martin, KUITHAN, Friederike, MOHR, Brigitte, FÜSSEL, Monika, OELSCHLÄGEL, Uta, THIEDE, Christian, RÖLLIG, Christoph, PLATZBECKER, Uwe, SCHETELIG, Johannes

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Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk... von Garcia-Pelaez, J, Barbosa-Matos, R, Lobo, S, Dias, A, Garrido, L, Castedo, S, Sousa, SP, Pinheiro, H, Sousa, L, Monteiro, AR, Maqueda, J, Fernandes, S, Carneiro, F, Pinto, N, Lemos, C, Pinto, C, Teixeira, M, Aretz, S, Lagercrantz, SB, Balmana, J, Blatnik, A, Benusiglio, P, Blanluet, M, Bours, V, Brems, H, Brunet, J, Calistri, D, Capella, G, Revilla, SC, Colas, C, Dahan, K, de Putter, R, Desseignes, C, Dominguez-Garrido, E, Egas, C, Evans, G, Feret, D, Fewings, E, Fitzgerald, R, Coulet, F, Garcia-Barcina, M, Genuardi, M, Lisa, G, Hackmann, K, Hanson, H, Holinski-Feder, E, Huneburg, R, Krajc, M, Lagerstedt-Robinson, K, Lazaro, C, Ligtenberg, M, Bouzas, MCM, Merino, S, Michils, G, Novakovic, S, Patino, A, Ranzani, G, Schrock, E, Silva, I, Silveira, C, Soto, JL, Spier, I, Steinke-Lange, V, Tedaldi, G, Tejada, I, Woodward, E, Tischkowitz, M, Hoogerbrugge, N, Oliveira, C

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Highly significant antiviral activity of HIV-1 LTR-specific tre-recombinase in humanized mice von Hauber, I, Hofmann-Sieber, H, Chemnitz, J, Dubrau, D, Chusainow, J, Stucka, R, Hartjen, P, Schambach, A, Ziegler, P, Hackmann, K, Schröck, E, Schumacher, U, Lindner, C, Grundhoff, A, Baum, C, Manz, M G, Buchholz, F, Hauber, J

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Molekulare Karyotypisierung in der genetischen Diagnostik: Technologien und Anwendungen von Hackmann, K., Engels, H., Schröck, E.

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Molekulare Karyotypisierung in der genetischen Diagnostik von Hackmann, K., Engels, H., Schröck, E.

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Clinical management of an atypical dental invagination von Badran, Zahi, Lopez-Cazaux, Serena, Crauste, Eléonore, Bray, Estelle, Soueidan, Assem, Armengol, Valérie

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Characterization of the Binding Protein-Dependent Cellobiose and Cellotriose Transport System of the Cellulose Degrader Streptomyces reticuli von SCHLÖSSER, A, JANTOS, J, HACKMANN, K, SCHREMPF, H

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Activity of the herbal combination, PC-SPES, in the treatment of patients with androgen-independent prostate cancer von Oh, William K, George, Daniel J, Hackmann, Kristin, Manola, Judith, Kantoff, Philip W

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A splice form of polycystin-2, lacking exon 7, does not interact with polycystin-1 von Hackmann, Karl, Markoff, Arseni, Qian, Feng, Bogdanova, Nadia, Germino, Gregory G., Pennekamp, Petra, Dworniczak, Bernd, Horst, Jürgen, Gerke, Volker

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