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Search Results - DIVRY, E.
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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.
Published in
Atherosclerosis
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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.
Published in
Atherosclerosis
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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.
Published in
Canadian metallurgical quarterly
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Application of Cathodoluminescence Technique in Light Microscopy to Crystallisation Study of Mold Fluxes
by
Paransky, E.
,
Divry, E.
,
Rigaud, M.
Published in
Microscopy and microanalysis
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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
Published in
Pediatrics (Evanston)
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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
Published in
Molecular genetics and metabolism
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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
Published in
Archives of disease in childhood
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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
Published in
Clinica chimica acta
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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
Published in
Archives of disease in childhood. Fetal and neonatal edition
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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
Published in
European journal of pediatrics
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Divry's Modern English-Greek and Greek-English Desk Dictionary
by
Rexine, John E.
Published in
The Modern language journal (Boulder, Colo.)
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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
Published in
European journal of pediatrics
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