Iterative Project Processes within Temporary Multi-Organizations in Construction: The Self-, Eco-, Re-Organizing Projects von de Blois, Michel, Lizarralde, Gonzalo, De Coninck, Pierre

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Cohérence et continuum d’accompagnement dans les écosystèmes éducatifs entrepreneuriaux von Lesage, Xavier, Jacquemin, Amélie, De Blois, Michel

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Structuring of temporary multi-organizations: Contingency theory in the building sector von Lizarralde, Gonzalo, Blois, Michel de, Latunova, Iskra

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Wood Cladding in Non-residential Construction: Overcoming the Barriers to Leverage the Opportunities von Guy-Plourde, Samuel, De Blois, Michel, Blanchet, Pierre, Barbuta, Costel, Robichaud, François

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Cladding Materials in Non-Residential Construction: Consideration Criteria for Stakeholder in the Province of Quebec von Samuel Guy-Plourde, Pierre Blanchet, Michel de Blois, Francois Robichaud, Costel Barbuta

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Biological deoxygenation method and uses thereof von De Blois, Michel

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Biological deoxygenation method and uses thereof von DE BLOIS MICHEL

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Biological deoxygenation method and uses thereof von DE BLOIS MICHEL

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BIOLOGICAL DEOXYGENATION METHOD AND USES THEREOF von DE BLOIS, MICHEL

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STRUCTURAL MEMBER von DE BLOIS, MICHEL, VALOIS, ANDRE

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BIOLOGICAL DEOXYGENATION METHOD AND USES THEREOF von DE BLOIS, MICHEL, VALOIS, ANDRE

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Contiguous Gene Deletion within Chromosome Arm 10q Is Associated with Juvenile Polyposis of Infancy, Reflecting Cooperation between the BMPR1A and PTEN Tumor-Suppressor Genes von Delnatte, Capucine, Sanlaville, Damien, Mougenot, Jean-François, Vermeesch, Joris-Robert, Houdayer, Claude, Blois, Marie-Christine de, Genevieve, David, Goulet, Olivier, Fryns, Jean-Pierre, Jaubert, Francis, Vekemans, Michel, Lyonnet, Stanislas, Romana, Serge, Eng, Charis, Stoppa-Lyonnet, Dominique

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Phenotype-genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature von Nizon, Mathilde, Andrieux, Joris, Rooryck, Caroline, de Blois, Marie-Christine, Bourel-Ponchel, Emilie, Bourgois, Béatrice, Boute, Odile, David, Albert, Delobel, Bruno, Duban-Bedu, Bénédicte, Giuliano, Fabienne, Goldenberg, Alice, Grotto, Sarah, Héron, Delphine, Karmous-Benailly, Houda, Keren, Boris, Lacombe, Didier, Lapierre, Jean-Michel, Le Caignec, Cédric, Le Galloudec, Eric, Le Merrer, Martine, Le Moing, Anne-Gaëlle, Mathieu-Dramard, Michèle, Nusbaum, Sylvie, Pichon, Olivier, Pinson, Lucile, Raoul, Odile, Rio, Marlène, Romana, Serge, Roubertie, Agnès, Colleaux, Laurence, Turleau, Catherine, Vekemans, Michel, Nabbout, Rima, Malan, Valérie

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Functional disomy of the Xq28 chromosome region von SANLAVILLE, Damien, PRIEUR, Marguerite, CORMIER-DAIRE, Valerie, BAUJAT, Genevieve, ROMANA, Serge, VEKEMANS, Michel, TURLEAU, Catherine, DE BLOIS, Marie-Christine, GENEVIEVE, David, LAPIERRE, Jean-Michel, OZILOU, Catherine, PICQ, Monique, GOSSET, Philippe, MORICHON-DELVALLEZ, Nicole, MUNNICH, Arnold

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Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome von De Leersnyder, Hélène, de Blois, Marie-Christine, Claustrat, Bruno, Romana, Serge, Albrecht, Urs, von Kleist-Retzow, Jürgen-Christoph, Delobel, Bruno, Viot, Géraldine, Lyonnet, Stanislas, Vekemans, Michel, Munnich, Arnold

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17q21.31 Microdeletion: Brain Anomalies Leading to Prenatal Diagnosis von Egloff, Matthieu, Encha-Razavi, Ferechte, Garel, Catherine, Bonnière-Darcy, Maryse, Millischer, Anne-Elodie, Lapierre, Jean-Michel, Fontaine, Sophie, de Blois, Marie-Christine, Vekemans, Michel, Turleau, Catherine, Ville, Yves, Malan, Valérie

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β1-adrenergic antagonists improve sleep and behavioural disturbances in a circadian disorder, Smith-Magenis syndrome von De Leersnyder, Hélène, de Blois, Marie-Christine, Vekemans, Michel, Sidi, Daniel, Villain, Elisabeth, Kindermans, Catherine, Munnich, Arnold

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Identification of the IRXB gene cluster as candidate genes in severe dysgenesis of the ocular anterior segment von Chaabouni, Myriam, Etchevers, Heather, De Blois, Marie Christine, Calvas, Patrick, Waill-Perrier, Marie Christine, Vekemans, Michel, Romana, Serge Pierrick

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A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation von Colleaux, L, Rio, M, Heuertz, S, Moindrault, S, Turleau, C, Ozilou, C, Gosset, P, Raoult, O, Lyonnet, S, Cormier-Daire, V, Amiel, J, Le Merrer, M, Picq, M, de Blois, M C, Prieur, M, Romana, S, Cornelis, F, Vekemans, M, Munnich, A

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Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature von Faivre, Laurence, Gosset, Philippe, Cormier-Daire, Valérie, Odent, Sylvie, Amiel, Jeanne, Giurgea, Irina, Nassogne, Marie-Cécile, Pasquier, Laurent, Munnich, Arnold, Romana, Serge, Prieur, Marguerite, Vekemans, Michel, De Blois, Marie-Christine, Turleau, Catherine

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