Claire-Lise Gervason < Claire-Marie Dhaenens < Clara Barbot

Facettes :

List of bibliographic references indexed by Claire-Marie Dhaenens

Number of relevant bibliographic references: 4.

Ident.	Authors (with country if any)	Title
002020 (2009)	Mélissa Yana Frédéric [France] ; Fabienne Clot [France] ; Arnaud Blanchard [France] ; Claire-Marie Dhaenens [France] ; Gaëtan Lesca [France] ; Laura Cif [France] ; Alexandra Dürr [France] ; Marie Vidailhet [France] ; Bernard Sablonniere [France] ; Alain Calender [France] ; Maria Martinez [France] ; Nicolas Molinari [France] ; Alexis Brice [France] ; Mireille Claustres [France] ; Sylvie Tuffery-Giraud [France] ; Gwenaëlle Collod-Beroud [France]	The p.Asp216His TOR1A allele effect is not found in the French population
002490 (2009)	Mélissa Yana Frederic [France] ; Fabienne Clot [France] ; Amaud Blanchard [France] ; Claire-Marie Dhaenens [France] ; Gaëtan Lesca [France] ; Laura Cif [France] ; Alexandra Dürr [France] ; Marie Vidailhet [France] ; Bernard Sablonniere [France] ; Alain Calender [France] ; Maria Martinez [France] ; Nicolas Molinari [France] ; Alexis Brice [France] ; Mireille Claustres [France] ; Sylvie Tuffery-Giraud [France] ; Gwenaëlle Collod-Beroud [France]	The p.Asp216His TOR1A Allele Effect Is Not Found in the French Population
003318 (2006)	David Devos [France] ; Isabelle Vuillaume [France] ; Alix De Becdelievre [France] ; Berengère De Martinville [France] ; Claire-Marie Dhaenens [France] ; Jean-Christophe Cuvellier [France] ; Jean-Marie Cuisset [France] ; Louis Vallée [France] ; Marie-Pierre Lemaitre [France] ; Hélène Bourteel [France] ; Eric Hachulla [France] ; Benoit Wallaert [France] ; Alain Destée [France] ; Luc Defebvre [France] ; Bernard Sablonnière [France]	New syndromic form of benign hereditary chorea is associated with a deletion of TITF‐1 and PAX‐9 contiguous genes
003979 (2005)	Claire-Marie Dhaenens [France] ; Pierre Krystkowiak [France] ; Xavier Douay [France] ; Pierre Charpentier [France] ; Sylvain Bele [France] ; Alain Destée [France] ; Bernard Sablonnière [France]	Clinical and genetic evaluation in a French population presenting with primary focal dystonia

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