Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome von Coupry, I, Roudaut, C, Stef, M, Delrue, M-A, Marche, M, Burgelin, I, Taine, L, Cruaud, C, Lacombe, D, Arveiler, B

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Mosaic maternal uniparental isodisomy for chromosome 7q21-qter von Reboul, M-P, Tandonnet, O, Biteau, N, Belet-de Putter, C, Rebouissoux, L, Moradkhani, K, Vu, PY, Saura, R, Arveiler, B, Lacombe, D, Taine, L, Iron, A

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Successful therapeutic effect in a mouse model of erythropoietic protoporphyria by partial genetic correction and fluorescence-based selection of hematopoietic cells von FONTANELLAS, A, MENDEZ, M, ENRIQUEZ DE SALAMANCA, R, DE VERNEUIL, H, MAZURIER, F, CARIO-ANDRE, M, NAVARRO, S, GED, C, TAINE, L, GERONIMI, F, RICHARD, E, MOREAU-GAUDRY, F

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Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation von GIRAUDEAU, FABIENNE, TAINE, LAURENCE, BIANCALANA, VALÉRIE, DELOBEL, BRUNO, JOURNEL, HUBERT, MISSIRIAN, CHANTAL, LACOMBE, DIDIER, BONNEAU, DOMINIQUE, PARENT, PHILIPPE, AUBERT, DOMINIQUE, HAUCK, YOLANDE, CROQUETTE, MARIE FRANÇOISE, TOUTAIN, ANNICK, MATTEI, MARIE GENEVIÈVE, LOISEAU, HERVÉ AVET, DAVID, ALBERT, VERGNAUD, GILLES

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Leucodystrophy and oculocutaneous albinism in a child with an 11q14 deletion von Coupry, Isabelle, Taine, Laurence, Goizet, Cyril, Soriano, Carine, Mortemousque, Bruno, Arveiler, Benoît, Lacombe, Didier

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Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplas... von BAHUAU, MICHEL, LAURENDEAU, INGRID, PELET, ANNA, ASSOULINE, BRIGITTE, LAMIREAU, THIERRY, TAINE, LAURENCE, LE BAIL, BRIGITTE, VERGNES, PIERRE, GALLET, SERGE, VIDAUD, MICHEL, LYONNET, STANISLAS, LACOMBE, DIDIER, VIDAUD, DOMINIQUE

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Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis : Analysis of four FRAXE families with mild mental retardation in males von BIANCALANA, V, TAINE, L, BOUIX, J.-C, FINCK, S, CHAUVIN, A, DE VERNEUIL, H, KNIGHT, S. J. L, STOLL, C, LACOMBE, D, MANDEL, J.-L

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Neoplastic cells do not carry bcl2-JH rearrangements detected in a subset of primary cutaneous follicle center B-cell lymphomas von VERGIER, Béatrice, BELAUD-ROTUREAU, Marc-Antoine, BENASSY, Marie-Noëlle, BEYLOT-BARRY, Marie, DUBUS, Pierre, DELAUNAY, Michelle, GARROSTE, Jean-Christophe, TAINE, F. Laurence, MERLIO, Jean-Philippe

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Analysis of CBP (CREBBP) gene deletions in Rubinstein-Taybi syndrome patients using real-time quantitative PCR von Coupry, Isabelle, Monnet, Laurence, Moneim Attia, Azza Abd El, Taine, Laurence, Lacombe, Didier, Arveiler, Benoît

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Prenatal diagnosis of trisomy 9. Six cases and a review of the literature von Saura, R., Traore, W., Taine, L., Wen, Z. Q., Roux, D., Maugey-Laulom, B., Ruffie, M., Vergnaud, A., Horovitz, J.

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False-negative results of trisomy 21 on direct analysis on chorionic villus sampling von Saura, R., Roux, D., Maugey-Laulon, B., Taine, L., Wen, Z. Q., Vergnaud, A., Horovitz, J.

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Safety and fetal outcome of early and midtrimester amniocentesis von Konje, Justin C, de Chazal, Richard, Abrams, Keith, Taylor, David J

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PRENATAL DIAGNOSIS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA BY METABOLIC MEASUREMENT AND DNA MUTATION ANALYSIS von GED, C., MOREAU-GAUDRY, F., TAINE, L., HOMBRADOS, I., CALVAS, P., COLOMBIES, P., DE VERNEUIL, H.

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Gene Therapy of a Mouse Model of Protoporphyria with a Self-Inactivating Erythroid-Specific Lentiviral Vector without Preselection von Richard, Emmanuel, Mendez, Manuel, Mazurier, Fréderic, Morel, Carine, Costet, Pierre, Xia, Ping, Fontanellas, Antonio, Geronimi, Fabien, Cario-André, Muriel, Taine, Laurence, Ged, Cecile, Malik, Punam, de Verneuil, Hubert, Moreau-Gaudry, François

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Prenatal diagnosis and management of sex chromosome aneuploidy: a report on 98 cases von Brun, Jean-Luc, Gangbo, Flore, Qi Wen, Zon, Galant, Katia, Taine, Laurence, Maugey-Laulom, Brigitte, Roux, Denis, Mangione, Raphaelle, Horovitz, Jacques, Saura, Robert

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Combination of WAGR and Potocki-Shaffer contiguous deletion syndromes in a patient with an 11p11.2-p14 deletion von Brémond-Gignac, Dominique, Crolla, John A, Copin, Henri, Guichet, Agnès, Bonneau, Dominique, Taine, Laurence, Lacombe, Didier, Baumann, Clarisse, Benzacken, Brigitte, Verloes, Alain

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Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH von Goizet, Cyril, Excoffier, Elsa, Taine, Laurence, Taupiac, Emmanuelle, El Moneim, Azza Abd, Arveiler, Benoit, Bouvard, Manuel, Lacombe, Didier

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Souvenirs de la Vie parisienne (3e éd.) / par Marcelin ; préf par H. Taine von Marcelin, Émile (1825-1887). Auteur du texte

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Voyages de Gulliver / par Jonathan Swift. Notice sur l'auteur / par Louise Lacuria von Swift, Jonathan (1667-1745). Auteur du texte, Lacuria, Louise. Auteur du texte

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A novel immunodeficient mouse model--RAG2 x common cytokine receptor gamma chain double mutants--requiring exogenous cytokine administration for human hematopoietic stem cell engra... von Mazurier, F, Fontanellas, A, Salesse, S, Taine, L, Landriau, S, Moreau-Gaudry, F, Reiffers, J, Peault, B, Di Santo, J P, de Verneuil, H

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