Syndromic Short Stature in Patients with a Germline Mutation in the LIM Homeobox LHX4
Machinis, Kalotina, Pantel, Jacques, Netchine, Irène, Léger, Juliane, Camand, Olivier J.A., Sobrier, Marie-Laure, Moal, Florence Dastot-Le, Duquesnoy, Philippe, Abitbol, Marc, Czernichow, Paul, Amselem, Serge
Published in American journal of human genetics (01.11.2001)
Published in American journal of human genetics (01.11.2001)
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Journal Article
Slits contribute to the guidance of retinal ganglion cell axons in the mammalian optic tract
Thompson, Hannah, Barker, David, Camand, Olivier, Erskine, Lynda
Published in Developmental biology (15.08.2006)
Published in Developmental biology (15.08.2006)
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Journal Article
Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the “Mowat–Wilson” syndrome
Bassez, Guillaume, Camand, Olivier J.A, Cacheux, Valère, Kobetz, Alexandra, Dastot-Le Moal, Florence, Marchant, Dominique, Catala, Martin, Abitbol, Marc, Goossens, Michel
Published in Neurobiology of disease (01.03.2004)
Published in Neurobiology of disease (01.03.2004)
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Journal Article
Mutational analysis of the OA1 gene in ocular albinism
Camand, Olivier, Boutboul, Sandrine, Gat, Laurence, Arbogast, Laurence, Roche, Olivier, Sternberg, Claude, Sutherland, Joanne, Levin, Alex, Héon, Elise, Menasche, Maurice, Dufier, Jean-Louis, Abitbol, Marc
Published in Ophthalmic genetics (01.09.2003)
Published in Ophthalmic genetics (01.09.2003)
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Journal Article
Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome
Vieira, Veronique, David, Gabriel, Roche, Olivier, de la Houssaye, Guillaume, Boutboul, Sandrine, Arbogast, Laurence, Kobetz, Alexandra, Orssaud, Christophe, Camand, Olivier, Schorderet, Daniel F, Munier, Francis, Rossi, Annick, Delezoide, Anne Lise, Marsac, Cecile, Ricquier, Daniel, Dufier, Jean-Louis, Menasche, Maurice, Abitbol, Marc
Published in Molecular vision (01.12.2006)
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Published in Molecular vision (01.12.2006)
Journal Article
Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the 'Mowat-Wilson'syndrome
Bassez, Guillaume, Camand, Olivier J A, Cacheux, Valere, Kobetz, Alexandra, Moal, Florence Dastot-Le, Marchant, Dominique, Catala, Martin, Abitbol, Marc, Goossens, Michel
Published in Neurobiology of disease (01.03.2004)
Published in Neurobiology of disease (01.03.2004)
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Journal Article
Embryonic expression of the leptin receptor gene in mesoderm-derived tissues
Camand, Olivier, Turban, Sophie, Abitbol, Marc, Guerre-Millo, Michèle
Published in Comptes rendus. Biologies (01.02.2002)
Published in Comptes rendus. Biologies (01.02.2002)
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Journal Article
Mutation analysis of the tyrosinase gene in oculocutaneous albinism: Mutations in Brief
Camand, Olivier, Marchant, Dominique, Boutboul, Sandrine, Péquignot, Marie, Odent, Sylvie, Dollfus, Hélène, Sutherland, Joanne, Levin, Alex, Menasche, Maurice, Marsac, Cécile, Dufier, Jean-Louis, Heon, Elise, Abitbol, Marc
Published in Human mutation (01.04.2001)
Published in Human mutation (01.04.2001)
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Journal Article
Mutation analysis of the tyrosinase gene in oculocutaneous albinism
Camand, Olivier, Marchant, Dominique, Boutboul, Sandrine, Péquignot, Marie, Odent, Sylvie, Dollfus, Hélène, Sutherland, Joanne, Levin, Alex, Menasche, Maurice, Marsac, Cécile, Dufier, Jean-Louis, Heon, Elise, Abitbol, Marc
Published in Human mutation (01.04.2001)
Published in Human mutation (01.04.2001)
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Journal Article