Cooking Up Fun! A Youth Development Strategy that Promotes Independent Food Skills von Thonney, Patricia F., Bisogni, Carole A.

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G.P.5.08 Myofibrillar myopathies: The Lausanne experience with DES mutations in 11 patients von Dunand, M, Lobrinus, J.A, Thonney, F, Jeanrenaud, X, Selcen, D, Rudnik-Schöneborn, S, Burgunder, J.M, Kuntzer, T

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Evidence of Somatic and Germinal Mosaicism in Pseudo–Low-Penetrant Hereditary Retinoblastoma, by Constitutional and Single-Sperm Mutation Analysis von Munier, Francis L., Thonney, Francine, Girardet, Anne, Balmer, Aubin, Claustre, Mireille, Pellestor, Frank, Senn, Alfred, Pescia, Graziano, Schorderet, Daniel F.

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Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patients von Bojinova, Rossiana I., Schorderet, Daniel F., Addor, Marie-Claude, Gaide, Anne-Claude, Thonney, Francine, Pescia, Graziano, Nenadov-Beck, Maja, Balmer, Aubin, Munier, Francis L.

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Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomalies von Lavanchy, Laure, Munier, Francis L., Cousin, Pascal, Gaide, Anne-Claude, Thonney, Francine, Schorderet, Daniel F.

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Fetus with two identical reciprocal translocations: Description of a rare complication of consanguinity von Martinet, Danielle, Vial, Yvan, Thonney, Francine, Beckmann, Jacques S., Meagher‐Villemure, Kathleen, Unger, Sheila

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Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastoma von Munier, F. L., Thonney, F., Balmer, A., Uffer, S., Héon, E., Melle, G. Van, Rutz, H. P., Pescia, G., Schorderet, D. F.

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Constitutional Karyotype in Retinoblastoma Case Report and Review of Literature von Munier, F., Balmer, A., Gailloud, C., Pescia, G., Jotterand-Bellomo, M., Thonney, F.

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A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype von HERGERSBERG, M, BALAKRISHNAN, J, THONNEY, F, MOSER, H, MALIK, N, BETTECKEN, T, CHEVALIER-PORST, F, BRÄGGER, C, BURGER, R, EINSCHENK, I, LIECHTI-GALLATI, S, MORRIS, M, SCHORDERET, D

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PATERNAL SELECTION FAVORING MUTANT ALLELES OF THE RETINOBLASTOMA SUSCEPTIBILITY GENE von MUNIER, F, SPENCE, MA, PESCIA, G, BALMER, A, GAILLOUD, C, THONNEY, F, VANMELLE, G, RUTZ, HP

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Residues of agricultural chemicals on fruits and vegetables: pesticide use and regulatory issues von Thonney, P.F. (Cornell University), Bisogni, C.A

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Clinical applications of molecular diagnosis of retinoblastoma ain 15 families von Lendi, B, Pescia, G, Thonney, F, Balmer, A, Munier, F

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Sex Mutation Ratio in Retinoblastoma and Retinoma: Relevance to Genetic Counseling von Munier, Francis L., Thonney, Francine, Balmer, Aubin, Héon, Elise, Pescia, Graziano, Schorderet, Daniel F.

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Association between haplotypes and specific mutations in Swiss cystic fibrosis families von LIECHTI-GALLATI, S, MALIK, N, ALKAN, M, MAECHLER, M, MORRIS, M, THONNEY, F, SENNHAUSER, F, MOSER, H

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Applications de l'hybridation in situ fluorescente (FISH) dans le diagnostic prénatal von Pescia, G., Fokstuen, S., Thonney, F.

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Applications of fluorescence in situ hybridization in prenatal diagnosis von Pescia, G, Fokstuen, S, Thonney, F

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Evaluation of a supermarket nutrition education program von Olson, Christine M., Bisogni, Carole A., Thonney, Patricia F.

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Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients von Munier, F, Balmer, A, von Moos, C, Pescia, G, Gailloud, C, van Melle, G, Thonney, F, Gaide, A C, Allaz, M J, Rutz, H P

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Applications cliniques du diagnostic moléculaire du rétinoblastome dans 15 familles von LENDI, B, PESCIA, G, THONNEY, F, BALMER, A, MUNIER, F

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Assisted fertilization in azoospermic men: results of CHUV from 1994 to 1997 von Wisard, M, Senn, A, Thonney, F, Schorderet, D F, Germond, M

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