New Mutations Associated with Rasopathies in a Central European Population and Genotype–Phenotype Correlations von Čizmárová, M., Hlinková, K., Bertok, S., Kotnik, P., Duba, H.C., Bertalan, R., Poločková, K., Košťálová, Ľ., Pribilincová, Z., Hlavatá, A., Kovács, L., Ilenčíková, D.

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Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D) von Vasen, H F A, Ghorbanoghli, Z, Bourdeaut, F, Cabaret, O, Caron, O, Duval, A, Entz-Werle, N, Goldberg, Y, Ilencikova, D, Kratz, C P, Lavoine, N, Loeffen, J, Menko, F H, Muleris, M, Sebille, G, Colas, C, Burkhardt, B, Brugieres, L, Wimmer, K

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Recurring multifocal leiomyosarcoma of the urinary bladder 22 years after therapy for bilateral (hereditary) retinoblastoma: a case report and review of the literature von Svajdler, Jr, M, Andrašina, I, Ilenčíková, D, Rychlý, B, Piačková, B

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Constitutional mismatch repair-deficiency syndrome (CMMR-D) - a case report of a family with biallelic MSH6 mutation von Ilenčíková, D

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New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype Correlations: Rasopathies in Central Europe von Čizmárová, M., Hlinková, K., Bertok, S., Kotnik, P., Duba, H.C., Bertalan, R., Poločková, K., Košťálová, Ľ., Pribilincová, Z., Hlavatá, A., Kovács, L., Ilenčíková, D.

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Rasopathies - dysmorphic syndromes with short stature and risk of malignancy von Cizmarova, M, Kostalova, L, Pribilincova, Z, Lasabova, Z, Hlavata, A, Kovacs, L, Ilencikova, D

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Clustering of mutations in the 5' tertile of the NF1 gene in Slovakia patients with optic pathway glioma von Bolcekova, A, Nemethova, M, Zatkova, A, Hlinkova, K, Pozgayova, S, Hlavata, A, Kadasi, L, Durovcikova, D, Gerinec, A, Husakova, K, Pavlovicova, Z, Holobrada, M, Kovacs, L, Ilencikova, D

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Late onset of familial neurogenic diabetes insipidus in monozygotic twins von Cizmarova, M, Nagyova, G, Janko, V, Pribilincova, Z, Virgova, D, Ilencikova, D, Kovacs, L

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Identification of molecular markers in children with acute myeloid leukemia (AML) von Ilenčíková, D, Sýkora, J, Mikulášová, Z, Repiská, V

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Complex Multidisciplinary Follow-Up Of Children With Neurofibromatosis Type 1 von Bolceková, A, Hlavatá, A, Zat, A 'ková, Némethová, M, Holobradá, M, Sýkora, P, Gerinec, A, Husáková, K, Ilencíková, D, Kovács, L

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Clinical dysmorphic syndromes with tumorigenesis von Ilenčíková, D, Cižmárová, M, Krajčiová, A, Požgayová, S, Rybárová, A, Kovács, L

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Burkitt lymphoma with unusual granulomatous reaction. A case report von Janegová, A, Janega, P, Ilencíková, D, Babál, P

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New insights to the MLL recombinome of acute leukemias von Meyer, C, Kowarz, E, Hofmann, J, Renneville, A, Zuna, J, Trka, J, Ben Abdelali, R, Macintyre, E, De Braekeleer, E, De Braekeleer, M, Delabesse, E, de Oliveira, M P, Cavé, H, Clappier, E, van Dongen, J J M, Balgobind, B V, van den Heuvel-Eibrink, M M, Beverloo, H B, Panzer-Grümayer, R, Teigler-Schlegel, A, Harbott, J, Kjeldsen, E, Schnittger, S, Koehl, U, Gruhn, B, Heidenreich, O, Chan, L C, Yip, S F, Krzywinski, M, Eckert, C, Möricke, A, Schrappe, M, Alonso, C N, Schäfer, B W, Krauter, J, Lee, D A, zur Stadt, U, Te Kronnie, G, Sutton, R, Izraeli, S, Trakhtenbrot, L, Lo Nigro, L, Tsaur, G, Fechina, L, Szczepanski, T, Strehl, S, Ilencikova, D, Molkentin, M, Burmeister, T, Dingermann, T, Klingebiel, T, Marschalek, R

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Clinical Laboratory Method for Detection of IGHV Mutation Status in Patients with CLL Validated by Igblast and IMGT/V-QUEST von Lasabova, Z., Plank, L., Flochova, E., Burjanivova, T., Vanochova, A., Mihok, L., Ilencikova, D.

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Targeted prostate cancer screening in men with mutations in BRCA1 and BRCA2 detects aggressive prostate cancer: preliminary analysis of the results of the IMPACT study von Mitra, Anita V., Bancroft, Elizabeth K., Barbachano, Yolanda, Page, Elizabeth C., Foster, C. S., Jameson, C., Mitchell, G., Lindeman, G. J., Stapleton, A., Suthers, G., Evans, D. G., Cruger, D., Blanco, I., Mercer, C., Kirk, J., Maehle, L., Hodgson, S., Walker, L., Izatt, L., Douglas, F., Tucker, K., Dorkins, H., Clowes, V., Male, A., Donaldson, A., Brewer, C., Doherty, R., Bulman, B., Osther, P. J., Salinas, M., Eccles, D., Axcrona, K., Jobson, I., Newcombe, B., Cybulski, C., Rubinstein, W. S., Buys, S., Townshend, S., Friedman, E., Domchek, S., Ramon y Cajal, T., Spigelman, A., Teo, S. H., Nicolai, N., Aaronson, N., Ardern‐Jones, A., Bangma, C., Dearnaley, D., Eyfjord, J., Falconer, A., Grönberg, H., Hamdy, F., Johannsson, O., Khoo, V., Kote‐Jarai, Z., Lilja, H., Lubinski, J., Melia, J., Moynihan, C., Peock, S., Rennert, G., Schröder, F., Sibley, P., Suri, M., Wilson, P., Bignon, Y. J., Strom, S., Tischkowitz, M., Liljegren, A., Ilencikova, D., Abele, A., Kyriacou, K., van Asperen, C., Kiemeney, L., Easton, D. F., Eeles, Rosalind A.

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The CHEK2 c.1100delC germline mutation rarely contributes to breast cancer development in the Czech Republic von KLEIBL, Zdenek, NOVOTNY, Jan, BEZDICKOVA, Drahomira, MALIK, Radek, KLEIBLOVA, Petra, FORETOVA, Lenka, PETRUZELKA, Lubos, ILENCIKOVA, Denisa, CINEK, Petr, POHLREICH, Petr

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Acute myeloblastic leukaemia with alternations of MLL proto-oncogene protein (11q23/MLL+ AML) von Mikulásová, Z, Ilencíková, D, Slamka, T, Durovcíková, D

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Multiplex SNaPshot genotyping for detecting loss of heterozygosity in the mismatch-repair genes MLH1 and MSH2 in microsatellite-unstable tumors von Bujalkova, M, Zavodna, K, Krivulcik, T, Ilencikova, D, Wolf, B, Kovac, M, Karner-Hanusch, J, Heinimann, K, Marra, Giancarlo, Jiricny, J, Bartosova, Z

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Spectrum of germ-line MLH1 and MSH2 mutations in Austrian patients with hereditary nonpolyposis colorectal cancer von Wolf, Brigitte, Henglmueller, Silvia, Janschek, Elisabeth, Ilencikova, Denisa, Ludwig-Papst, Carmen, Bergmann, Michael, Mannhalter, Christine, Wrba, Friedrich, Karner-Hanusch, Judith

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Novel MLH1 and MSH2 germline mutations in the first HNPCC families identified in Slovakia von Bartosova, Z, Fridrichova, I, Bujalkova, M, Wolf, B, Ilencikova, D, Krizan, P, Hlavcak, P, Palaj, J, Lukac, L, Lukacova, M, Böör, A, Haider, R, Jiricny, J, Nyström-Lahti, M, Marra, Giancarlo

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