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C Pécheux

Showing results (1-10 of 5) with videos related to

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Clinical Genetics|December 14, 2011
Validation of comparative genomic hybridization arrays for the detection of genomic rearrangements of the calpain-3 and dysferlin genesM Bartoli, P Nègre, N Wein, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 26, 1999
Fibrinogen A alpha chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French familyL Hamidi Asl, V Fournier, C Billerey, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 2017
[Next-generation DNA sequencing in clinical diagnostics]C Lacoste, A Fabre, C Pécheux, et al.
Clinical Genetics|November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decayM Krahn, C Pécheux, F Chapon, et al.
Clinical Genetics|January 6, 2011
Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?M Krahn, M Goicoechea, F Hanisch, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Clinical Genetics|December 14, 2011
Validation of comparative genomic hybridization arrays for the detection of genomic rearrangements of the calpain-3 and dysferlin genesM Bartoli, P Nègre, N Wein, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 26, 1999
Fibrinogen A alpha chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French familyL Hamidi Asl, V Fournier, C Billerey, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 2017
[Next-generation DNA sequencing in clinical diagnostics]C Lacoste, A Fabre, C Pécheux, et al.
Clinical Genetics|November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decayM Krahn, C Pécheux, F Chapon, et al.
Clinical Genetics|January 6, 2011
Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?M Krahn, M Goicoechea, F Hanisch, et al.
Pageof 1