Chromosome 11p15 Paternal Isodisomy in Focal Forms of Neonatal Hyperinsulinism von Damaj, L., le Lorch, M., Verkarre, V., Werl, C., Hubert, L., Nihoul-Fékété, C., Aigrain, Y., de Keyzer, Y., Romana, S. P., Bellanne-Chantelot, C., de Lonlay, P., Jaubert, F.

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Terminal 14q32.33 deletion: Genotype–phenotype correlation von Maurin, M‐L., Brisset, S., Le Lorc'h, M., Poncet, V., Trioche, P., Aboura, A., Labrune, P., Tachdjian, G.

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Molecular cytogenetic characterization of a 4p15.1‐pter duplication and a 4q35.1‐qter deletion in a recombinant of chromosome 4 pericentric inversion von Maurin, M‐L., Labrune, P., Brisset, S., Le Lorc'h, M., Pineau, D., Castel, C., Romana, S., Tachdjian, G.

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809 Intradermal injection of bone marrow-MSC corrects recessive dystrophic epidermolysis bullosa in a xenograft model von Ganier, C., Titeux, M., Gaucher, S., Peltzer, J., Le Lorch, M., Lataillade, J., Ishida-Yamamoto, A., Hovnanian, A.

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Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasma von Alberti, A., Salomon, L. J., Le Lorc'h, M., Couloux, A., Bussières, L., Goupil, S., Malan, V., Pelletier, E., Hyon, C., Vialard, F., Rozenberg, P., Bouhanna, P., Oury, J. F., Schmitz, T., Romana, S., Weissenbach, J., Vekemans, M., Ville, Y.

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A CGH study of 27 patients with CHARGE association von 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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Molecular and Phenotypic Characterization of Ring Chromosome 22 in Two Unrelated Patients von Hannachi, H., Mougou, S., Benabdallah, I., Soayh, N., Kahloul, N., Gaddour, N., Le Lorc'h, M., Sanlaville, D., El Ghezal, H., Saad, A.

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Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genes von 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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Comparison of human skeletal myoblasts and bone marrow-derived CD133+progenitors for the repair of infarcted myocardium von Agbulut, Onnik, Vandervelde, Susanne, Al Attar, Nawwar, Larghero, Jérôme, Ghostine, Said, Léobon, Bertrand, Robidel, Estelle, Borsani, Paolo, Le Lorc'h, Marc, Bissery, Alvine, Chomienne, Christine, Bruneval, Patrick, Marolleau, Jean-Pierre, Vilquin, Jean-Thomas, Hagège, Albert, Samuel, Jane-Lyse, Menasché, Philippe

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Classical West “syndrome” phenotype with a subtelomeric 4p trisomy von Gérard‐Blanluet, Marion, Romana, S., Munier, C., Le Lorc'h, M., Kanafani, S., Sinico, M., Touboul, C., Levaillant, J.M., Haddad, B., Lopez, N., Lelong, F., de Villemeur, T. Billette, Verloes, A., Borghi, E.

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Can cold or heat shock improve skeletal myoblast engraftment in infarcted myocardium? von MAUREL, Agnès, AZARNOUSH, Kasra, BRUNEVAL, Patrick, HAGEGE, Alain, CARPENTIER, Alain, VILQUIN, Jean-Thomas, MENASCHE, Philippe, SABBAH, Laurent, VIGNIER, Nicolas, LE LORC'H, Marc, MANDET, Chantal, BISSERY, Alvine, GARCIN, Isabelle, CARRION, Claire, FISZMAN, Marc

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Assisting reproduction of infertile men carrying a Robertsonian translocation von Frydman, Nelly, Romana, Serge, Le Lorc'h, Marc, Vekemans, Michel, Frydman, René, Tachdjian, Gérard

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Posters Reproductive Genetics (PGD/PGS) von Crippa, A., Magli, M. C., Robles, F., Capoti, A., Ferraretti, A. P., Gianaroli, L., Gallina, A., Bonaparte, E., Moretti, M., Colpi, G. M., Nerva, F., Contalbi, G., Vacalluzzo, L., Tabano, S., Grati, F. R., Gazzano, G., Sirchia, S. M., Simoni, G., Miozzo, M., Handyside, A., Gabriel, A., Thornhill, A. R., Clemente, E., Reitter, C., Affara, N., Griffin, D. K., Macek, M., Feldmar, P., Kluckova, H., Hrehorcak, M., Diblik, J., Paulasova, P., Turnovec, M., Vilimova, S., Fontes, L., Haddad, L., Borges, E., Iaconelli, A., Braga, D. P. A. F., Vianna-Morgante, A. M., Komsky, A., Kasterstein, E., Komarovsky, D., Bern, O., Maslansky, B., Kaplan, T., Raziel, A., Friedler, S., Gidoni, Y., Ben-Ami, I., Ron-El, R., Strassburger, D., Maggiulli, R., Monahan, D., Neri, Q. V., Hu, J. C. Y., Rosenwaks, Z., Palermo, G. D., Beyazyurek, C., Ekmekci, G. C., Tac, H. A., Ajredin, N., Verlinsky, O., Fiorentino, F., Kahraman, S., Camp, M., Hesters, L., Le Lorc'h, M., Frydman, R., Romana, S., Frydman, N., Perez Sanz, J., Matorras, R., Arluzea, J., Romin, Y., Bilbao, J., Gonzalez-Santiago, N., Manova-Todorova, K., Koff, A., Rivera-Pomar, J. M., de la Hoz-Torres, C., Xanthopoulou, L., Ghevaria, H., Mantzouratou, A., Serhal, P., Doshi, A., Delhanty, J. D., Ye, Y., Qian, Y., Jin, F., Munne, S., Gutierrez, C., Wagner, C., Hill, D., Wiemer, K., Fischer, J., Kaplan, B., Danzer, H., Surrey, M., Opsahl, M.

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O▪87 Contribution of probes in preimplantation diagnosis of Robertsonian translocations von Le Lorc'h, M, Tachdjian, G, Frydman, N, Frydman, R, Vekemans, M, Romana, S

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A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances von Lapierre, J-M, Sanlaville, D, Kang, J, Ozilou, C, Le Lorc'h, M, Waill, M-C, Prieur, M, Colleaux, L, Munnich, A, Turleau, C, Benkhalifa, M, Mohammed, M, Vekemans, M, Romana, S

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Molecular Cytogenetic Characterization of a 4p 15.1-pter Duplication and a 4q35.1-qter Deletion in a Recombinant of Chromosome 4 Pericentric Inversion von MAURIN, M-L, LABRUNE, P, BRISSET, S, LE LORC'H, M, PINEAU, D, CASTEL, C, ROMANA, S, TACHDJIAN, G

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Per-urethral transvesical first-trimester amniocentesis von Frydman, R., Pons, J.C., Borghi, E., Selva, J., Olivennes, F., O'Donovan, F., Fernandez, H., Le Lorc'h, M.

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Pure partial 7p trisomy including the TWIST,HOXA, and GLI3genes von MÉGARBANÉ, A, LE LORC'H, M, ELGHEZAL, H, JOLY, G, GOSSET, P, SOURATY, N, SAMARAS, L, PRIEUR, M, VEKEMANS, M, TURLEAU, C, ROMANA, S P

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Molecular cytogenetic characterization of a 4p15.1-pter duplication and a 4q35.1-qter deletion in a recombinant of chromosome 4 pericentric inversion von Maurin, M-L., Labrune, P., Brisset, S., Le Lorc'h, M., Pineau, D., Castel, C., Romana, S., Tachdjian, G.

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Terminal 14q32.33 deletion: Genotype-phenotype correlation von Maurin, M-L., Brisset, S., Le Lorc'h, M., Poncet, V., Trioche, P., Aboura, A., Labrune, P., Tachdjian, G.

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