Study of aneuploidy and DNA fragmentation in gametes of patients with severe teratozoospermia von Perrin, A, Louanjli, N, Ziane, Y, Louanjli, T, Le Roy, C, Gueganic, N, Amice, V, De Braekeleer, M, Morel, F

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Decrease of spermatozoa with an unbalanced chromosome content after cell sorting in men carrying a structural chromosomal abnormality von El Fekih, S., Tous, C., Gueganic, N., Brugnon, F., Ali, H. Ben, Bujan, L., Moinard, N., Caire‐Tetauru, E., Ajina, M., Douet‐Guilbert, N., Morel, F., 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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DNA fragmentation is higher in spermatozoa with chromosomally unbalanced content in men with a structural chromosomal rearrangement von Perrin, A., Nguyen, M. H., Bujan, L., Vialard, F., Amice, V., Guéganic, N., Douet‐Guilbert, N., Braekeleer, M., Morel, F.

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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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Decrease of spermatozoa with an unbalanced chromosome content after cell sorting in men carrying a structural chromosomal abnormality von El Fekih, S., Tous, C., Gueganic, N., Brugnon, F., Ali, H. Ben, Bujan, L., Moinard, N., Caire‐tetauru, E., Ajina, M., Douet‐guilbert, N., Morel, F., Perrin, A.

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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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Del(5q) and MLL amplification in homogeneously staining region in acute myeloblastic leukemia: a recurrent cytogenetic association von Herry, Angèle, Douet-Guilbert, Nathalie, Guéganic, Nadia, Morel, Frédéric, Le Bris, Marie-Josée, Berthou, Christian, De Braekeleer, Marc

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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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SOR SAVOIR PATIENT. Comprendre le cancer de l'ovaire : information à l'usage des personnes malades et de leurs proches von  ,  

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