PRODH mutations and hyperprolinemia in a subset of schizophrenic patients von Jacquet, Hélène, Raux, Grégory, Thibaut, Florence, Hecketsweiler, Bernadette, Houy, Emmanuelle, Demilly, Caroline, Haouzir, Sadeq, Allio, Gabrielle, Fouldrin, Gael, Drouin, Valérie, Bou, Jacqueline, Petit, Michel, Campion, Dominique, Frébourg, Thierry

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Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum von Campion, Dominique, Dumanchin, Cécile, Hannequin, Didier, Dubois, Bruno, Belliard, Serge, Puel, Michèle, Thomas-Anterion, Catherine, Michon, Agnès, Martin, Cosette, Charbonnier, Françoise, Raux, Grégory, Camuzat, Agnès, Penet, Christiane, Mesnage, Valérie, Martinez, Maria, Clerget-Darpoux, Françoise, Brice, Alexis, Frebourg, Thierry

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Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene von BOUGEARD, Gaëlle, BRUGIERES, Laurence, FREBOURG, Thierry, CHOMPRET, Agnès, GESTA, Paul, CHARBONNIER, Francoise, VALENT, Alexander, MARTIN, Cosette, RAUX, Grégory, FEUNTEUN, Jean, BRESSAC-DE PAILLERETS, Brigitte

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Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome von Raux, Grégory, Bumsel, Emilie, Hecketsweiler, Bernadette, van Amelsvoort, Therese, Zinkstok, Janneke, Manouvrier-Hanu, Sylvie, Fantini, Carole, Brévière, Georges-Marie M., Di Rosa, Gabriella, Pustorino, Giuseppina, Vogels, Annick, Swillen, Ann, Legallic, Solenn, Bou, Jacqueline, Opolczynski, Gaelle, Drouin-Garraud, Valérie, Lemarchand, Marie, Philip, Nicole, Gérard-Desplanches, Aude, Carlier, Michèle, Philippe, Anne, Nolen, Marie Christine, Heron, Delphine, Sarda, Pierre, Lacombe, Didier, Coizet, Cyril, Alembik, Yves, Layet, Valérie, Afenjar, Alexandra, Hannequin, Didier, Demily, Caroline, Petit, Michel, Thibaut, Florence, Frebourg, Thierry, Campion, Dominique

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Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short f... von CHARBONNIER, F, RAUX, G, QING WANG, DROUOT, N, CORDIER, F, LIMACHER, J.-M, SAURIN, J.-C, PUISIEUX, A, OLSCHWANG, S, FREBOURG, T

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Distribution ofENG andACVRL1 (ALK1) mutations in French HHT patients von Lesca, Gaëtan, Burnichon, Nelly, Raux, Grégory, Tosi, Mario, Pinson, Stéphane, Marion, Marie-Jeanne, Babin, Emmanuel, Gilbert-Dussardier, Brigitte, Rivière, Sophie, Goizet, Cyril, Faivre, Laurence, Plauchu, Henri, Frébourg, Thierry, Calender, Alain, Giraud, Sophie

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Acd, a peptidoglycan hydrolase of Clostridium difficile with N-acetylglucosaminidase activity von Dhalluin, Anne, Bourgeois, Ingrid, Pestel-Caron, Martine, Camiade, Emilie, Raux, Gregory, Courtin, Pascal, Chapot-Chartier, Marie-Pierre, Pons, Jean-Louis

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APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy von Brice, Alexis, Hannequin, Didier, Laquerrière, Annie, Dumanchin, Cécile, Vercelletto, Martine, Campion, Dominique, Feuillette, Sébastien, Meur, Nathalie Le, Raux, Gregory, Rovelet-Lecrux, Anne, Frebourg, Thierry, Vital, Anne, Dubas, Frédéric

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A Simple Method for the Routine Detection of Somatic Quantitative Genetic Alterations in Colorectal Cancer von Killian, Audrey, Di Fiore, Frédéric, Le Pessot, Florence, Blanchard, France, Lamy, Aude, Raux, Grégory, Flaman, Jean–Michel, Paillot, Bernard, Michel, Pierre, Sabourin, Jean–Christophe, Tuech, Jean–Jacques, Michot, Francis, Kerckaert, Jean–Pierre, Sesboüé, Richard, Frebourg, Thierry

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Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients von Lesca, Gaëtan, Burnichon, Nelly, Raux, Grégory, Tosi, Mario, Pinson, Stéphane, Marion, Marie-Jeanne, Babin, Emmanuel, Gilbert-Dussardier, Brigitte, Rivière, Sophie, Goizet, Cyril, Faivre, Laurence, Plauchu, Henri, Frébourg, Thierry, Calender, Alain, Giraud, Sophie

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Deleterious mutations in exon 1 of  MECP2 in Rett syndrome von Quenard, Aline, Yilmaz, Saliha, Fontaine, Hervé, Bienvenu, Thierry, Moncla, Anne, des Portes, Vincent, Rivier, François, Mathieu, Michèle, Raux, Grégory, Jonveaux, Philippe, Philippe, Christophe

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Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation von Maréchal, Lucie, Raux, Grégory, Dumanchin, Cécile, Lefebvre, Guillaume, Deslandre, Emmanuelle, Girard, Carole, Campion, Dominique, Parain, Dominique, Frebourg, Thierry, Hannequin, Didier

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Analysis of the allele-specific expression of the mismatch repair gene MLH1 using a simple DHPLC-Based Method von Tournier, Isabelle, Raux, Grégory, Fiore, Fréderic Di, Maréchal, Isabelle, Leclerc, Carole, Martin, Cosette, Wang, Qing, Buisine, Marie-Pierre, Stoppa-Lyonnet, Dominique, Olschwang, Sylviane, Frébourg, Thierry, Tosi, Mario

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Analysis of the allele-specific expression of the mismatch repair gene MLH1 using a simple DHPLC-Based Method: Allele-Specific Expression Measured By DHPLC von Tournier, Isabelle, Raux, Grégory, Fiore, Fréderic Di, Maréchal, Isabelle, Leclerc, Carole, Martin, Cosette, Wang, Qing, Buisine, Marie-Pierre, Stoppa-Lyonnet, Dominique, Olschwang, Sylviane, Frébourg, Thierry, Tosi, Mario

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KIT AND METHOD FOR IN VITRO DETECTION OF RHESUS D von RAUX, GRÉGORY

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A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24 von Ber, Isabelle Le, Martinez, Maria, Campion, Dominique, Laquerrière, Annie, Bétard, Christine, Bassez, Guillaume, Girard, Carol, Saugier-Veber, Pascale, Raux, Gregory, Sergeant, Nicolas, Magnier, Patrick, Maisonobe, Thierry, Eymard, Bruno, Duyckaerts, Charles, Delacourte, André, Frebourg, Thierry, Hannequin, Didier

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KIT AND METHOD FOR IN VITRO DETECTION OF RHESUS D von RAUX, GRÉGORY

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Comparison of a Quantitative PCR Method with FISH for the Assessment of the Four Aneuploïdies Commonly Evaluated in CLL Patients von Bastard, Christian, Fruchart, Christophe, Raux, Gregory, Parmentier, Francoise, Vaur, Dominique, Tilly, Herve

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Comparison of a Quantitative PCR Method with FISH for the Assessment of the Four Aneuploïdies Commonly Evaluated in CLL Patients von Bastard, Christian, Fruchart, Christophe, Raux, Gregory, Parmentier, Francoise, Vaur, Dominique, Tilly, Herve

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Association of KM Genotype with Bullous Pemphigoid von Raux, Grégory, Gilbert, Danièle, Joly, Pascal, Daveau, Maryvonne, Martel, Philippe, Christ, Marielle, Tron, François

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