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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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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Dual NRASQ61R and BRAFV600E mutation-specific immunohistochemistry completes molecular screening in melanoma samples in a routine practice von Uguen, Arnaud, MD, Guéguen, Paul, MD, Legoupil, Delphine, MD, Bouvier, Stéphanie, Costa, Sebastian, MD, Duigou, Sandrine, Lemasson, Gilles, MD, Ledé, Françoise, MD, Sassolas, Bruno, MD, Talagas, Matthieu, MD, Férec, Claude, MD, PhD, Le Maréchal, Cédric, MD, PhD, De Braekeleer, Marc, MD, PhD, Marcorelles, Pascale, MD, PhD

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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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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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Azoospermie : prise en charge et résultats. À propos de 90 cas von Coat, C., Perrin, A., Talagas, M., Tetefort, R., Amice, J., Valéri, A., De Braekeleer, M., Amice, V.

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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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Genetic epidemiology of autosomal recessive spastic ataxia of Charlevoix-Saguenay in northeastern Quebec von De Braekeleer, M., Giasson, F., Mathieu, J., Roy, M., Bouchard, J. P., Morgan, K.

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Disease knowledge in a high-risk population for cystic fibrosis von Braekeleer, M D, Bellis, G, Rault, G, Allard, C, Milot, M, Simard, F

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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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Double minutes containing amplified bcr‐abl fusion gene in a case of chronic myeloid leukemia treated by imatinib von Morel, Frédéric, Bris, Marie‐Josée Le, Herry, Angèle, Calvez, Geneviève Le, Marion, Véronique, Abgrall, Jean‐François, Berthou, Christian, Braekeleer, Marc De

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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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A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec von MERANTE, F, PETROVA-BENEDICT, R, MACKAY, N, MITCHELL, G, LAMBERT, M, MORIN, C, DE BRAEKELEER, M, LAFRAMBOISE, R, GAGNE, R, ROBINSON, R. H

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New insights to the MLL recombinome of acute leukemias von MEYER, C, KOWARZ, E, DELABESSE, E, DE OLIVEIRA, M. P, CAVE, H, CLAPPIER, E, VAN DONGEN, Jjm, BALGOBIND, B. V, VAN DEN HEUVEL-EIBRINK, M. M, BEVERLOO, H. B, PANZER-GRÜMAYER, R, TEIGLER-SCHLEGEL, A, HOFMANN, J, HARBOTT, J, KJELDSEN, E, SCHNITTGER, S, KOEHL, U, GRUHN, B, HEIDENREICH, O, CHAN, L. C, YIP, S. F, KRZYWINSKI, M, ECKERT, C, RENNEVILLE, A, 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, ZUNA, J, TRAKHTENBROT, L, LO NIGRO, L, TSAUR, G, FECHINA, L, SZCZEPANSKI, T, STREHL, S, ILENCIKOVA, D, MOLKENTIN, M, BURMEISTER, T, DINGERMANN, T, TRKA, J, KLINGEBIEL, T, MARSCHALEK, R, BEN ABDELAII, R, MACINTYRE, E, DE BRAEKELEER, E, DE BRAEKELEER, M

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Linkage results on 11Q21-22 in Eastern Quebec pedigrees densely affected by schizophrenia von Maziade, M., Raymond, V., Cliche, D., Fournier, J. P., Caron, C., Garneau, Y., Nicole, L., Marcotte, P., Couture, C., Simard, C., Boivin, R., Rodrigue, C., Boutin, P., De Braekeleer, M., Martinez, M., Mérette, C.

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Mucoviscidose et fecondite des couples porteurs du gene au Saguenay: Lac-Saint-Jean (Quebec, Canada) von Braekeleer, Marc De, Bellis, Gil, Gaimard, Maryse, Rault, Gilles, Milot, Marcel, Simard, Fernand

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Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern Quebec von DE BRAEKELEER, M, DALLAIRE, A, MATHIEU, J

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Mucoviscidose et fécondité des couples porteurs du gène au Saguenay: Lac-Saint-Jean (Québec, Canada) von De Braekeleer, Marc, Bellis, Gil, Gaimard, Maryse, Rault, Gilles, Milot, Marcel, Simard, Fernand

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Little phenotypic variability in three CF sibs compound heterozygous for the 621 + 1G→T and the 711 + 1G→T mutations von DE BRAEKELEER, M, SIMARD, F, AUBIN, G

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Incidence of Cystic Fibrosis in Saguenay-Lac-St.-Jean (Quebec, Canada) von DAIGNEAULT, JOCELYNE, AUBIN, GERVAIS, SIMARD, FERNAND, DE BRAEKELEER, MARC

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