Rossier, Colette

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Journal Article

Makrythanasis, Periklis; Kapranov, Philipp; Bartoloni, Lucia; Reymond, Alexandre; Deutsch, Samuel; Guigo, Roderic; Denoeud, France; Drenkow, Jorg; Rossier, Colette; Ariani, Francesca; Capra, Valeria; Excoffier, Laurent; Renieri, Alessandra; Gingeras, Thomas R.; Antonarakis, Stylianos E. (2009). Variation in Novel Exons (RACEfrags) of the MECP2 Gene in Rett Syndrome Patients and Controls. Human mutation, 30(9), E866 - E879. Hoboken, N.J.: Wiley-Blackwell 10.1002/humu.21073

Failly, Mike; Saitta, Alexandra; Muñoz, Analia; Falconnet, Emilie; Rossier, Colette; Santamaria, Francesca; de Santi, Maria Margherita; Lazor, Romain; DeLozier-Blanchet, Celia D; Bartoloni, Lucia; Blouin, Jean-Louis (2008). DNAI1 mutations explain only 2% of primary ciliary dykinesia. Respiration, 76(2), pp. 198-204. Basel: Karger 10.1159/000128567

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