The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion by ROMANA, S. P, MAUCHAUFFE, M, LE CONIAT, M, CHUMAKOV, I, LE PASLIER, D, BERGER, R, BERNARD, O. A

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High Frequency of t(12;21) in Childhood B-Lineage Acute Lymphoblastic Leukemia by Romana, S.P., Poirel, H., Leconiat, M., Flexor, M.-A., Mauchauffé, M., Jonveaux, P., Macintyre, E.A., Berger, R., Bernard, O.A.

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PMX2B, a new candidate gene for Hirschsprung's disease by Benailly, HK, Lapierre, JM, Laudier, B, Amiel, J, Attié, T, De Blois, MC, Vekemans, M, Romana, SP

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Sotos syndrome caused by a paracentric inversion disrupting the NSD1 gene by Malan, V, De Blois, MC, Prieur, M, Perrier-Waill, MC, Huguet-Nedjar, C, Gegas, L, Turleau, C, Vekemans, M, Munnich, A, Romana, SP

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Molecular karyotyping in human constitutional cytogenetics by Sanlaville, Damien, Lapierre, Jean-Michel, Turleau, Catherine, Coquin, Aurélie, Borck, Guntram, Colleaux, Laurence, Vekemans, Michel, Romana, Serge Pierrick

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Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype by Joly, G, Lapierre, J-M, Ozilou, C, Gosset, P, Aurias, A, De Blois, M-C, Prieur, M, Raoul, O, Colleaux, L, Munnich, A, Romana, SP, Vekemans, M, Turleau, C

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Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genes by MEGARBANE, A, LE LORC'H, M, ROMANA, S. P, ELGHEZAL, H, JOLY, G, GOSSET, P, SOURATY, N, SAMARAS, L, PRIEUR, M, VEKEMANS, M, TURLEAU, C

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A CGH study of 27 patients with CHARGE association by Sanlaville, D, Romana, SP, Lapierre, JM, Amiel, J, Genevieve, D, Ozilou, C, Le Lorch, M, Brisset, S, Gosset, P, Baumann, C, Turleau, C, Lyonnet, S, Vekemans, M

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Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis by Elghezal, Hatem, Le Guyader, Gaëlle, Radford-Weiss, Isabella, Perot, Christine, Van Den Akker, Jacqueline, Eydoux, Patrice, Vekemans, Michel, Romana, Serge P.

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Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features by Fert-Ferrer, Sandra, Guichet, Agnès, Tantau, Julia, Lise Delezoide, Anne, Ozilou, Catherine, Pierrick Romana, Serge, Gosset, Philippe, Viot, Géraldine, Loison, Stéphane, Moraine, Claude, Morichon-Delvallez, Nicole, Turleau, Catherine, Vekemans, Michel, Prieur, Marguerite

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A cryptic chromosome 19 abnormality in a patient with Ph-positive acute lymphoblastic leukemia by Berger, Roland, Busson, Maryvonne, Romana, Serge P.

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Acute megakaryoblastic leukemia and loss of the RUNX1 gene by Berger, Roland, Busson, Maryvonne, Dastugue, Nicole, Radford-Weiss, Isabelle, Michaux, Lucienne, Hagemeijer, Anne, Quilichini, Benoît, Benattar, Laurence, Bernard, Olivier, Romana, Serge P.

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Identical abnormality of the short arm of chromosome 18 in two Philadelphia-positive chronic myelocytic leukemia patients with erythroblastic transformation, resulting in duplicati... by Khac, Florence Nguyen, Waill, Marie-Christine, Romana, Serge P, Radford-Weiss, Isabelle, Busson, Maryvonne, Collonge-Rame, Marie-Agnès, Ribadeau-Dumas, Antoine, Piffaut, Marie-Claude, Daniel, Marie-Thérèse, Davi, Frédéric, Merle-Béral, Hélène, Berger, Roland, Arock, Michel

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Microarray CGH: principle and use for constitutional disorders by Sanlaville, D, Lapierre, J M, Coquin, A, Turleau, C, Vermeesch, J, Colleaux, L, Borck, G, Vekemans, M, Aurias, A, Romana, S P

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