Aneuploidy and DNA Fragmentation in Sperm of Carriers of a Constitutional Chromosomal Abnormality von Perrin, A., Basinko, A., Douet-Guilbert, N., Gueganic, N., Le Bris, M.-J., Amice, V., De Braekeleer, M., Morel, F.

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Molecular characterization of deletions of the long arm of chromosome 5 (del(5q)) in 94 MDS/AML patients von Douet-Guilbert, N, De Braekeleer, E, Basinko, A, Herry, A, Gueganic, N, Bovo, C, Trillet, K, Dos Santos, A, Le Bris, M J, Morel, F, Eveillard, J R, Berthou, C, De Braekeleer, M

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A study of meiotic segregation of chromosomes in spermatozoa of translocation carriers using fluorescent in situ hybridisation von Perrin, A., Morel, F., Douet-Guilbert, N., Le Bris, M.-J., Amice, J., Amice, V., De Braekeleer, M.

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Chromosome aneuploidy in the spermatozoa of two men with globozoospermia von Morel, F., Douet-Guilbert, N., Moerman, A., Duban, B., Marchetti, C., Delobel, B., Le Bris, M.-J., Amice, V., De Braekeleer, M.

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Fluorescence in situ hybridization characterization of ider(20q) in myelodysplastic syndrome von Douet‐Guilbert, N., Laï, J. L., Basinko, A., Gueganic, N., Andrieux, J., Pollet, B., Plantier, I., Delattre, C., Crépin, O., Corm, S., Le Bris, M. J., Morel, F., De Braekeleer, M.

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A new partner gene fused to ABL1 in a t(1;9)(q24;q34)-associated B-cell acute lymphoblastic leukemia von De Braekeleer, E, Douet-Guilbert, N, Le Bris, M-J, Berthou, C, Morel, F, De Braekeleer, M

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Balanced complex chromosome rearrangement in male infertility: case report and literature review von Nguyen, M. H., Morel, F., Pennamen, P., Parent, P., Douet-Guilbert, N., Le Bris, M. J., Basinko, A., Roche, S., De Braekeleer, M., Perrin, A.

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Segregation of chromosomes in sperm of a t(X;18)(q11;p11.1) carrier inherited from his mother: Case Report von Perrin, A., Douet-Guilbert, N., Le Bris, M.J., Keromnes, G., Langlois, M.L., Barrière, P., Amice, J., Amice, V., De Braekeleer, M., Morel, F.

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Écrire Éducation à l’Université von Serra, Enric, Universitat Autònoma de Barcelona. Servei de Llengües, Universitat de Barcelona. Serveis Lingüístics, Universitat de Girona. Servei de Llengües Modernes, Universitat de Lleida. Institut de Llengües, Universitat Abat Oliva CEU. Servei de Llengües

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Interchromosomal effect in sperm of males with translocations: report of 6 cases and review of the literature von DOUET-GUILBERT, N., BRIS, M.-J. L., AMICE, V., MARCHETTI, C., DELOBEL, B., AMICE, J., BRAEKELEER, M. D., MOREL, F.

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HReMAS: hybrid real-time musical alignment system von Cabañas-Molero, P., Cortina-Parajón, Raquel, Combarro, E. F., Alonso, Pedro, Bris-Peñalver, F. J.

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Molecular cytogenetics of IGH rearrangements in non-Hodgkin B-cell lymphoma von Bernicot, I., Douet-Guilbert, N., Le Bris, M.-J., Herry, A., Morel, F., De Braekeleer, M.

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Meiotic segregation in spermatozoa of a 45,XY,-14,der(18)t(14;18)(q11;p11.3) translocation carrier: A Case Report von Perrin, A., Douet-Guilbert, N., Laudier, B., Couet, M.L., Guérif, F., Royère, D., Le Bris, M.J., De Braekeleer, M., Morel, F.

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Clonal chromosomal abnormalities in the Philadelphia chromosome negative cells of chronic myeloid leukemia patients treated with imatinib von Guilbert-Douet, N, Morel, F, Bris, M-J Le, Berthou, C, Morice, P, Bourquard, P, Braekeleer, M D

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Lack of intraindividual variation of unbalanced spermatozoa frequencies from a 46,XY,t(9;22)(q21;q11.2) carrier: Case report von Morel, F., Douet-Guilbert, N., Le Bris, M.-J., Herry, A., Marchetti, C., Lefebvre, V., Delobel, B., Amice, V., Amice, J., De Braekeleer, M.

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A street deposit sampling method for metal and hydrocarbon contamination assessment von Bris, François-Jérôme, Garnaud, Stéphane, Apperry, Nicole, Gonzalez, Ana, Mouchel, Jean-Marie, Chebbo, Ghassan, Thévenot, Daniel R

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18p trisomy: A case of direct 18p duplication characterized by molecular cytogenetic analysis von Marical, H., Le Bris, M.J., Douet-Guilbert, N., Parent, P., Descourt, J.P., Morel, F., De Braekeleer, M.

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Detection of an unexpected subtelomeric 15q26.2 → qter deletion in a little girl: Clinical and cytogenetic studies von Pinson, L., Perrin, A., Plouzennec, C., Parent, P., Metz, C., Collet, M., Le Bris, M.J., Douet‐Guilbert, N., Morel, F., De Braekeleer, M.

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Isolated granulocytic sarcoma followed by acute myelogenous leukemia type FAB-M2 associated with inversion 16 and trisomies 9 and 22 von MOREL, F, HERRY, A, LE BRIS, M-J, LE CALVEZ, G, MARION, V, BERTHOU, C, DE BRAEKELEER, M

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Isoderivative of deleted chromosome 20 in primary myelofibrosis (PMF) characterized by molecular cytogenetics and array CGH von Douet-Guilbert, N, Andrieux, J, Laï, J. L, Morice, P, Demory, J. L, Basinko, A, Ugo, V, Gueganic, N, Le Bris, M. J, Morel, F, De Braekeleer, M

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