A syndromic form of X-linked mental retardation: the Coffin-Lowry syndrome von TOURAINE, Renaud-Laurian, ZENIOU, Maria, HANAUER, André

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A 13-bp deletion (1952 del 13) in the methylmalonyl CoA mutase gene of an affected patient von Touraine, Renaud-Laurian, Rolland, Marie-Odile, Divry, Priscille, Mathieu, Monique, Guibaud, Pierre, Bozon, Dominique

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Chronic neuromyotonia as a phenotypic variation associated with a new mutation in the KCNA1 gene von Poujois, A, Antoine, J-Ch, Combes, A, Touraine, R L

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Y chromosome microdeletion screening in infertile men in France:a survey of French practice based on 88 IVF centres von Aknin‐Seifer, Isabelle Esther, Lejeune, Hervé, Touraine, Renaud Laurian, Levy, Rachel

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