Deletions Overlapping VCAN Exon 8 Are New Molecular Defects for Wagner Disease von Burin‐des‐Roziers, Cyril, Rothschild, Pierre‐Raphael, Layet, Valérie, Chen, Jian‐Min, Ghiotti, Tiffany, Leroux, Céline, Cremers, Frans P. M., Brézin, Antoine P., Valleix, Sophie

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De Novo Splice Mutation in the Versican Gene in a Family With Wagner Syndrome von Rothschild, Pierre-Raphaël, Audo, Isabelle, Nedelec, Brigitte, Ghiotti, Tiffany, Brézin, Antoine P, Monin, Claire, Valleix, Sophie

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A family with Wagner syndrome with uveitis and a new versican mutation von Rothschild, Pierre-Raphaël, Brézin, Antoine P, Nedelec, Brigitte, Burin des Roziers, Cyril, Ghiotti, Tiffany, Orhant, Lucie, Boimard, Mathieu, Valleix, Sophie

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Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes von Vasson, Aurélie, Leroux, Céline, Orhant, Lucie, Boimard, Mathieu, Toussaint, Aurélie, Leroy, Chrystel, Commere, Virginie, Ghiotti, Tiffany, Deburgrave, Nathalie, Saillour, Yoann, Atlan, Isabelle, Fouveaut, Corinne, Beldjord, Cherif, Valleix, Sophie, Leturcq, France, Dodé, Catherine, Bienvenu, Thierry, Chelly, Jamel, Cossée, Mireille

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De novo splice mutation in the versican gene in a family with Wagner syndrome von Rothschild, Pierre-Raphaël, Audo, Isabelle, Nedelec, Brigitte, Ghiotti, Tiffany, Brézin, Antoine P, Monin, Claire, Valleix, Sophie

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