Additive effect of APOE rare variants on the phenotype of familial hypercholesterolemia by Marmontel, O., Khalil, Y. Abou, Bluteau, O., Cariou, B., Carreau, V., Charrière, S., Divry, E., Moulin, P., Peretti, N., Rabès, J.-P., Varret, M., Carrié, A., Di Filippo, M.

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Evaluation of new polygenic risk scores in the diagnosis of familial hypobetalipoproteinemia by Vanhoye, X., Rimbert, A., Moulin, P., Bardel, C., Rollat-Farnier, P.-A., Muntaner, M., Marmontel, O., Peretti, N., Fournier, C., Pichelin, M., Charrière, S., Divry, E., Chatelain, C., Meirhaeghe, A., Cariou, B., Di Filippo, M.

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THE INFLUENCE OF CHEMICAL COMPOSITION ON THE CRYSTALLIZATION AND THE HEAT TRANSFER OF SYNTHETIC MOULD FLUXES by VERMEULEN, Y., DIVRY, E., RIGAUD, M.

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Application of Cathodoluminescence Technique in Light Microscopy to Crystallisation Study of Mold Fluxes by Paransky, E., Divry, E., Rigaud, M.

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Clinical and biochemical phenotype in 11 patients with mevalonic aciduria by HOFFMANN, G. F, CHARPENTIER, C, TREFZ, F. K, RATING, D, BREMER, H. J, NYHAN, W. L, MAYATEPEK, E, MANCINI, J, LEICHSENRING, M, GIBSON, K. M, DIVRY, P, HREBICEK, M, LEHNERT, W, SARTOR, K

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Seventeen novel mutations that cause profound biotinidase deficiency by Wolf, B, Jensen, K, Hüner, G, Demirkol, M, Baykal, T, Divry, P, Rolland, M.-O, Perez-Cerdá, C, Ugarte, M, Straussberg, R, Basel-Vanagaite, L, Baumgartner, E.R, Suormala, T, Scholl, S, Das, A.M, Schweitzer, S, Pronicka, E, Sykut-Cegielska, J

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A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency by Touma, E H, Rashed, M S, Vianey-Saban, C, Sakr, A, Divry, P, Gregersen, N, Andresen, B S

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Plasma free fatty acids in mitochondrial fatty acid oxidation defects by Martı́nez, G, Jiménez-Sánchez, G, Divry, P, Vianey-Saban, C, Riudor, E, Rodés, M, Briones, P, Ribes, A

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A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency by Touma, E H, Rashed, M S, Vianey-Saban, C, Sakr, A, Divry, P, Gregersen, N, Andresen, B S

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Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus material by Kvittingen, E A, Guibaud, P P, Divry, P, Mandon, G, Rolland, M O, Domenichini, Y, Jakobs, C, Christensen, E

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Divry's Modern English-Greek and Greek-English Desk Dictionary by Rexine, John E.

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Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus material by Kvittingen, E A, Guibaud, P P, Divry, P, Mandon, G, Rolland, M O, Domenichini, Y, Jakobs, C, Christensen, E

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