نتائج البحث - Marie‐Claude Babron
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Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis حسب Benôıt Marin, Farid Boumédiène, Giancarlo Logroscino, Philippe Couratier, Marie‐Claude Babron, Anne‐Louise Leutenegger, Massimiliano Copetti, Pierre‐Marie Preux, Ettore Beghi
منشور في 2016Revisão -
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A second locus for Marfan syndrome maps to chromosome 3p24.2–p25 حسب Gwenaëlle Collod‐Béroud, Marie‐Claude Babron, Guillaume Jondeau, M Coulon, Jean Weissenbach, Olivier Dubourg, Jean‐Pierre Bourdarias, Catherine Bonaïti‐Pellié, Claudine Junien, Cathérine Boileau
منشور في 1994Artigo -
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Meta and pooled analysis of European coeliac disease data حسب Marie‐Claude Babron, Staffan Nilsson, Svetlana Adamovic, Åsa Torinsson Naluai, Jan Wahlström, Henry Ascher, Paul J. Ciclitira, Ludvig M. Sollid, Jukka Partanen, Luigi Greco, Françoise Clerget‐Darpoux
منشور في 2003Artigo -
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Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families حسب L. Greco, Marie‐Claude Babron, Gino Roberto Corazza, Selvaggia Percopo, R.E.P. Sica, F. Clot, M. C. FULCHIGNONI‐LATAUD, Patrizia Zavattari, Patricia Momigliano‐Richiardi, Giorgio Casari, Paolo Gasparini, Roberto Tosi, Vilma Mantovani, S. De Virgiliis, Giuseppe Iacono, Anna D’Alfonso, Hana Selinger‐Leneman, Arnaud Lemainque, J. L. Serre, Françoise Clerget‐Darpoux
منشور في 2001Artigo -
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Genome Search in Celiac Disease حسب Luigi Greco, Gino Roberto Corazza, Marie‐Claude Babron, Fabienne Clot, Marie-Claude Fulchignoni-Lataud, Selvaggia Percopo, Patrizia Zavattari, F. Bouguerra, Colette Dib, Roberto Tosi, Riccardo Bonfanti, Alessandro Ventura, Wilma Mantavoni, Giuseppe Magazzù, Rosanna Gatti, R Lazzari, Annamaria Giunta, Francesco Perri, Giuseppe Iacono, E Cardi, S. De Virgiliis, F Cataldo, Gianluigi De Angelis, S Musumeci, Roberto Ferrari, Fiorella Balli, Maria Teresa Bardella, Umberto Volta, Carlo Catassi, Giuliano Torre, Jean François Eliaou, Jean Louis Serre, Françoise Clerget‐Darpoux
منشور في 1998Artigo -
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Pleiotropic Effects of CEP290 (NPHP6) Mutations Extend to Meckel Syndrome حسب Lekbir Baala, Sophie Audollent, Jéléna Martinovic, Catherine Ozilou, Marie‐Claude Babron, Sivanthiny Sivanandamoorthy, Sophie Saunier, Rémi Salomon, Marie Gonzalès, Eleanor Rattenberry, Chantal Esculpavit, Annick Toutain, Claude Moraine, Philippe Parent, Pascale Marcorelles, Marie‐Christine Dauge, J. Roume, Martine Le Merrer, Vardiella Meiner, Karen Meir, Françoise Ménez, A. M. Beaufrére, Christine Francannet, Julia Tantau, Martine Sinico, Yves Dumez, Fiona MacDonald, Arnold Münnich, Stanislas Lyonnet, Marie‐Claire Gubler, Emmanuelle Génin, Colin A. Johnson, Michel Vekemans, Férechté Encha‐Razavi, Tania Attié‐Bitach
منشور في 2007Artigo -
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Refining genetic associations in multiple sclerosis حسب David R. Booth, Robert Heard, Graeme J. Stewart, An Goris, Rita Dobosi, Bénédicte Dubois, Annette Oturai, Helle Bach Søndergaard, Finn Sellebjerg, Janna Saarela, Virpi Leppä, Aarno Palotie, L. Peltonen, B. Fontaine, Isabelle Cournu‐Rebeix, Françoise Clerget‐Darpoux, Marie‐Claude Babron, Frank Weber, Herta Flor, Bertram Müller‐Myhsok, Peter Rieckmann, Antje Kroner, Colin A. Graham, Koen Vandenbroeck, Stanley Hawkins, Sandra D’Alfonso, Laura Bergamaschi, Paola Naldi, Franca Rosa Guerini, Marco Salvetti, Daniela Galimberti, Rogier Q. Hintzen, Cornelia M. van Duijn, Åslaug Rudjord Lorentzen, Elisabeth Gulowsen Celius, Hanne F. Harbo, Anne Spurkland, Francesco Cucca, Maria Giovanna Marrosu, Manuel Comabella, Xavier Montalbán, Pablo Villoslada, Tomas Olsson, Ingrid Kockum, Jan Hillert, Maria Ban, Andrew Walton, S. Sawcer, Alastair Compston, Clive Hawkins, Tania Mihalova, Neil P. Robertson, Gillian Ingram, Philip L. De Jager, David A. Hafler, John D. Rioux, Mark J. Daly, Lisa F. Barcellos, Adrian J. Ivinson, Margaret A. Pericak‐Vance, J. Hoksenberg, Stephen L. Hauser, Jacob L. McCauley, David Sexton, Jonathan L. Haines
منشور في 2008Carta
أدوات البحث:
موضوعات ذات صلة
Medicine
Biology
Gene
Genetics
Internal medicine
Disease
Physics
Genetic linkage
Incidence (geometry)
Meta-analysis
Amyotrophic lateral sclerosis
Antigen
Chromosome
Coeliac disease
Environmental health
Genome
Genome-wide association study
Genotype
Human leukocyte antigen
Linkage (software)
Locus (genetics)
Mathematics
Optics
Population
Single-nucleotide polymorphism
Antibody
Astrophysics
Bayesian probability
Bioinformatics
Centimorgan