نتائج البحث - Anne Philippe
- يعرض 1 - 11 نتائج من 11
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Ultrasonographic Pattern of Testicular Metastasis of Clear Cell Renal Cell Carcinoma with Pathological Correlation حسب Libert, Florent, Cabri-Wiltzer, Mathieu, Dardenne, Emmanuel, Draguet, Anne-Philippe, Puttemans, Thierry
منشور في 2016نص -
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Absorbed dose, equivalent dose, measured dose rates, and implications for OSL age estimates: Introducing the Average Dose Model حسب Guillaume Guérin, Catherine Christophe, Anne Philippe, Andrew Murray, Kristina J. Thomsen, Chantal Tribolo, Petra Urbanová, Mayank Jain, Pierre Guibert, Norbert Mercier, Sebastian Kreutzer, Christelle Lahaye
منشور في 2017Artigo -
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Levels of autistic traits in anorexia nervosa: a comparative psychometric study حسب Annaïg Courty, Anne Solène Maria, Christophe Lalanne, Damien Ringuenet, C. Vindreau, Coralie Chevallier, Lydia Pouga, François Pinabel, Anne Philippe, Jean‐Louis Adrien, Caroline Barry, Sylvie Berthoz
منشور في 2013Artigo -
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Profiling olfactory stem cells from living patients identifies miRNAs relevant for autism pathophysiology حسب Lam Son Nguyen, Marylin Lepleux, M. Makhlouf, Christelle Martin, Julien Fregeac, Karine Siquier-Pernet, Anne Philippe, François Féron, Bruno Gepner, Claire Rougeulle, Yann Humeau, Laurence Colleaux
منشور في 2016Artigo -
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Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder حسب Catalina Betancur, Marilys Corbex, Cécile Spielewoy, Anne Philippe, Jean Laplanche, J.M. Launay, Christopher Gillberg, MC Mouren-Siméoni, M. Hamon, Bruno Giros, Marika Nosten‐Bertrand, Marion Leboyer
منشور في 2002Artigo -
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Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder حسب Catalina Betancur, Marilys Corbex, Cécile Spielewoy, Anne Philippe, Jean Laplanche, J.M. Launay, Christopher Gillberg, MC Mouren-Siméoni, M. Hamon, Bruno Giros, Marika Nosten‐Bertrand, Marion Leboyer
منشور في 2002Artigo -
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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders حسب M-L Jacquemont, Damien Sanlaville, Richard Redon, O Raoul, Valérie Cormier‐Daire, Stanislas Lyonnet, Jeanne Amiel, M Le Merrer, D. Héron, M‐C De Blois, M Prieur, Michel Vekemans, N P Carter, A Munnich, Laurence Colleaux, Anne Philippe
منشور في 2006Artigo -
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Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech حسب Céline Bonnet, Joris Andrieux, Mylène Béri‐Dexheimer, B. Leheup, O. Boute, S. Manouvrier, B Delobel, H. Copin, Aline Receveur, M Mathieu, G. Thiriez, C. Le Caignec, A. David, M. C. de Blois, Valérie Malan, Anne Philippe, Valérie Cormier‐Daire, Laurence Colleaux, E. Flori, Hélène Dollfus, V. Pelletier, Christel Thauvin‐Robinet, A. Masurel-Paulet, L. Faivre, Marc Tardieu, Nadia Bahi‐Buisson, Patrick Callier, Francine Mugneret, Patrick Edery, Philippe Jonveaux, Damien Sanlaville
منشور في 2010Artigo -
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A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 حسب Robin Walters, Sébastien Jacquemont, Armand Valsesia, Adam J. de Smith, Danielle Martinet, Johanna C. Andersson‐Assarsson, Mario Falchi, Fei Chen, Joris Andrieux, Stéphane Lobbens, B Delobel, Fanny Stutzmann, Julia S. El-Sayed Moustafa, Jean-Claude Chèvre, Cécile Lecœur, Vincent Vatin, Sonia Bouquillon, Jessica L. Buxton, Odile Boute, Muriel Holder‐Espinasse, Jean‐Marie Cuisset, M. Lemaître, Anne‐Emmanuelle Ambresin, Andrea Brioschi, Muriel Gaillard, Vittorio Giusti, Florence Fellmann, Alessandra Ferrarini, Nouchine Hadjikhani, Dominique Campion, Audrey Guilmatre, Anna Goldenberg, Nadège Calmels, Jean‐Louis Mandel, Cédric Le Caignec, A. David, Bertrand Isidor, Marie‐Pierre Cordier, Sophie Dupuis‐Girod, Audrey Labalme, Damien Sanlaville, Mylène Béri‐Dexheimer, Philippe Jonveaux, Bruno Leheup, Katrin Õunap, Elena G. Bochukova, Elana Henning, Julia M. Keogh, Richard J. Ellis, K D MacDermot, Mieke M. van Haelst, C. Vincent‐Delorme, Ghislaine Plessis, Renaud Touraine, Anne Philippe, Valérie Malan, M. Mathieu‐Dramard, Jean Chiésa, Bettina Blaumeiser, R. Frank Kooy, Robert Caïazzo, Marie Pigeyre, Beverley Balkau, Robert Sladek, Sven Bergmann, Vincent Mooser, Dawn Waterworth, Alexandre Reymond, Péter Vollenweider, Gérard Waeber, Ants Kurg, Priit Palta, Tõnu Esko, Andres Metspalu, Mari Nelis, Paul Elliott, Anna‐Liisa Hartikainen, Mark I. McCarthy, L. Peltonen, Lena Carlsson, Peter Jacobson, Lars Sjöström, Ni Huang, Matthew E. Hurles, Stephen O’Rahilly, I. Sadaf Farooqi, Katrin Männik, Marjo‐Riitta Järvelin, François Pattou, Stephen Eyre, Andrew J. Walley, Lachlan Coin, Alexandra I. F. Blakemore, Philippe Froguel, J. Beckmann
منشور في 2010Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Psychiatry
Autism
Medicine
Bioinformatics
Genotype
Psychology
Copy-number variation
Genome
Phenotype
Single-nucleotide polymorphism
Autism spectrum disorder
Chromosome
Comparative genomic hybridization
Computational biology
Environmental health
Gene expression
Genetic heterogeneity
Linkage disequilibrium
Neuroscience
Population
Receptor
Serotonin transporter
Transmission disequilibrium test
5-HTTLPR
Abnormality
Absorbed dose
Alexithymia