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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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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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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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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236 Molecular characterization of deletion of the long arm of chromosome 5 (del5q) in 86 MDS/AML patients von Douet-Guilbert, N, De Braekeleer, E, Basinko, A, Herry, A, Gueganic, N, Bovo, C, Le Bris, M.-J, Morel, F, 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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Using Bacterial Artificial Chromosomes in Leukemia Research : The Experience at the University Cytogenetics Laboratory in Brest, France von De Braekeleer, Etienne, Douet-Guilbert, Nathalie, Basinko, Audrey, Morel, Frédéric, Le Bris, Marie-Josée, Férec, Claude, De Braekeleer, Marc

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Gene Expression Profiling of Adult t(4;11)(q21;q23)-associated Acute Lymphoblastic Leukemia Reveals a Different Signature from Pediatric Cases von DE BRAEKELEER, Etienne, DOUET-GUILBERT, Nathalie, LE BRIS, Marie-Josee, BASINKO, Audrey, MOREL, Frederic, DE BRAEKELEER, Marc

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Double Inv(3)(q21q26), a rare but recurrent chromosomal abnormality in myeloid hemopathies von De Braekeleer, Etienne, Douet-Guilbert, Nathalie, Le Bris, Marie-Josee, Ianotto, Jean-Christophe, Berthou, Christian, Gueganic, Nadia, Bovo, Clement, Basinko, Audrey, Morel, Frederic, De Braekeleer, Marc

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Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics von Douet-Guilbert, N, Basinko, A, Le Bris, M-J, Herry, A, Morel, F, De Braekeleer, M

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Stratégies d’identification des marqueurs chromosomiques surnuméraires en cytogénétique constitutionnelle von Douet-Guilbert, N., Basinko, A., Le Bris, M.-J., Herry, A., Morel, F., De Braekeleer, M.

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Stratégies d'identification des marqueurs chromosomiques surnuméraires en cytogénétique constitutionnelle: Génétique von DOUET-GUILBERT, N, BASINKO, A, LE BRIS, M.-J, HERRY, A, MOREL, F, 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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CDKN2C Deletion on 1p32 Locus As Part of Irwazh Score, a New Risk Assessment Model for Venous Thromboembolism Occurring within 6-12 Months of Treatment Initiation in Newly Diagnose... von Eveillard, Jean-Richard, Douet-Guilbert, Nathalie, Basinko, Audrey, Kerdoncuff, Romuald, Tempescul, Adrian, Saad, Hussam, Bekara, Charazed, Bezagu, Zoé, Eniafe-Eveillard, Moriamo, Nicol, Christophe, Ianotto, Jean-Christophe

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ETV6 fusion genes in hematological malignancies: A review von De Braekeleer, Etienne, Douet-Guilbert, Nathalie, Morel, Frédéric, Le Bris, Marie-Josée, Basinko, Audrey, De Braekeleer, Marc

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A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH von Poirsier, Céline, Besseau-Ayasse, Justine, Schluth-Bolard, Caroline, Toutain, Jérôme, Missirian, Chantal, Le Caignec, Cédric, Bazin, Anne, de Blois, Marie Christine, Kuentz, Paul, Catty, Marie, Choiset, Agnès, Plessis, Ghislaine, Basinko, Audrey, Letard, Pascaline, Flori, Elisabeth, Jimenez, Mélanie, Valduga, Mylène, Landais, Emilie, Lallaoui, Hakima, Cartault, François, Lespinasse, James, Martin-Coignard, Dominique, Callier, Patrick, Pebrel-Richard, Céline, Portnoi, Marie-France, Busa, Tiffany, Receveur, Aline, Amblard, Florence, Yardin, Catherine, Harbuz, Radu, Prieur, Fabienne, Le Meur, Nathalie, Pipiras, Eva, Kleinfinger, Pascale, Vialard, François, Doco-Fenzy, Martine

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Tailored Digital PCR Follow-Up of Rare Fusion Transcripts after Initial Detection through RNA Sequencing in Hematological Malignancies von Boulland, Marie-Laure, Aliouat, Amyra, Jalaber, Elie, Desmares, Anne, Toujani, Saloua, Luque Paz, Damien, Wiber, Margaux, Voirin, Emeline, Lachot, Sébastien, Basinko, Audrey, Lambert, Wayne-Corentin, Carras, Sylvain, Cousin, Elie, Marchand, Tony, de Tayrac, Marie, Fest, Thierry, Houot, Roch, Pastoret, Cédric

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Asian Population Is More Prone to Develop High-Risk Myelodysplastic Syndrome, Concordantly with Their Propensity to Exhibit High-Risk Cytogenetic Aberrations von Jiang, Yan, Eveillard, Jean-Richard, Couturier, Marie-Anne, Soubise, Benoit, Chen, Jian-Min, Gao, Sujun, Basinko, Audrey, Morel, Frederic, Douet-Guilbert, Nathalie, Troadec, Marie-Berengere

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3q26/EVI1 rearrangements in myeloid hemopathies: a cytogenetic review von De Braekeleer, Marc, Le Bris, Marie-Josée, De Braekeleer, Etienne, Basinko, Audrey, Morel, Frédéric, Douet-Guilbert, Nathalie

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Acute myeloid leukaemia (FAB AML‐M4Eo) with cryptic insertion of cbfb resulting in cbfb‐Myh11 fusion von Douet‐Guilbert, Nathalie, Chauveau, Aurelie, Gueganic, Nadia, Guillerm, Gaëlle, Tous, Corine, Le Bris, Marie‐Josee, Basinko, Audrey, Morel, Frederic, Ugo, Valerie, De Braekeleer, Marc

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