Resultados de procura - Sylvain Bolay
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1
Mutations in CNNM4 Cause Recessive Cone-Rod Dystrophy with Amelogenesis Imperfecta por Bozena Polok, Pascal Escher, Aude Ambresin, Éliane Chouery, Sylvain Bolay, Isabelle Meunier, Francis Nan, Christian Hamel, Francis L. Munier, Bernard Thilo, André Mégarbané, Daniel F. Schorderet
Publicado 2009Artigo -
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Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family por Pascal Escher, Peter Gouras, Raphaël Roduit, Leila Tiab, Sylvain Bolay, T. Delarive, Shiming Chen, Chih-Cheng Tsai, Masanori Hayashi, Jana Zernant, Joanna E. Merriam, Nicolas Mermod, Rando Allikmets, Francis L. Munier, Daniel F. Schorderet
Publicado 2008Artigo