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Charlène Chaix

Showing results (1-10 of 6) with videos related to

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Cancer Biomarkers : Section a of Disease Markers|November 2, 2016
Molecular combing: A new tool in diagnosing leukemiaAntoine Ittel, Hélène Zattara, Charlène Chaix, et al.
Human Mutation|March 13, 2018
Tricho-Hepato-Enteric Syndrome mutation update: Mutations spectrum of TTC37 and SKIV2L, clinical analysis and future prospectsPatrice Bourgeois, Clothilde Esteve, Charlène Chaix, et al.
American Journal of Medical Genetics. Part A|February 1, 2018
A new mutation in the C-terminal end of TTC37 leading to a mild form of syndromic diarrhea/tricho-hepato-enteric syndrome in seven patients from two familiesAlexandre Fabre, Laetitia-Marie Petit, Lars F Hansen, et al.
Annals of Neurology|October 27, 2011
Molecular combing reveals allelic combinations in facioscapulohumeral dystrophyKarine Nguyen, Pierre Walrafen, Rafaëlle Bernard, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
Inflammatory facioscapulohumeral muscular dystrophy type 2 in 18p deletion syndromeDimitri Renard, Guillaume Taieb, Matteo Garibaldi, et al.
Human Mutation|July 27, 2017
Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophyKarine Nguyen, Francesca Puppo, Stéphane Roche, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Cancer Biomarkers : Section a of Disease Markers|November 2, 2016
Molecular combing: A new tool in diagnosing leukemiaAntoine Ittel, Hélène Zattara, Charlène Chaix, et al.
Human Mutation|March 13, 2018
Tricho-Hepato-Enteric Syndrome mutation update: Mutations spectrum of TTC37 and SKIV2L, clinical analysis and future prospectsPatrice Bourgeois, Clothilde Esteve, Charlène Chaix, et al.
American Journal of Medical Genetics. Part A|February 1, 2018
A new mutation in the C-terminal end of TTC37 leading to a mild form of syndromic diarrhea/tricho-hepato-enteric syndrome in seven patients from two familiesAlexandre Fabre, Laetitia-Marie Petit, Lars F Hansen, et al.
Annals of Neurology|October 27, 2011
Molecular combing reveals allelic combinations in facioscapulohumeral dystrophyKarine Nguyen, Pierre Walrafen, Rafaëlle Bernard, et al.
American Journal of Medical Genetics. Part A|July 29, 2018
Inflammatory facioscapulohumeral muscular dystrophy type 2 in 18p deletion syndromeDimitri Renard, Guillaume Taieb, Matteo Garibaldi, et al.
Human Mutation|July 27, 2017
Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophyKarine Nguyen, Francesca Puppo, Stéphane Roche, et al.
Pageof 1