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S Tuffery

Showing results (1-10 of 43) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2016
[Genetics and molecular aspects of dystrophinopathies]F Leturcq, S Tuffery-Giraud
Ophthalmic Genetics|July 27, 1999
No missense mutation in choroideremia patients analyzed to dateL Beaufrère, M Claustres, S Tuffery
Human Mutation|January 1, 1992
A new intragenic polymorphism detected by the single-strand conformation polymorphism (SSCP) assay in the dystrophin geneS Tuffery, J Demaille, M Claustress
European Journal of Human Genetics : EJHG|January 1, 1996
Four novel dystrophin point mutations: detection by protein truncation test and transcript analysis in lymphocytes from Duchenne muscular dystrophy patientsS Tuffery, C Bareil, J Demaille, et al.
Human Genetics|May 1, 1995
Identification of variable length polyadenosine tract at the dystrophin locusS Tuffery, P Moine, J Demaille, et al.
Human Mutation|January 1, 1993
Base substitutions in the human dystrophin gene: detection by using the single-strand conformation polymorphism (SSCP) techniqueS Tuffery, P Moine, J Demaille, et al.
Annales De Biologie Clinique|August 5, 1999
[Genotypic diagnosis of Duchenne and Becker muscular dystrophies]S Tuffery-Giraud, S Chambert, J Demaille, et al.
Human Mutation|October 26, 1999
Point mutations in the dystrophin gene: evidence for frequent use of cryptic splice sites as a result of splicing defectsS Tuffery-Giraud, S Chambert, J Demaille, et al.
Journal Francais D'Ophtalmologie|October 6, 1998
[Retinoblastoma: importance of genetic counseling]A Girardet, L Beaufrere, S Tuffery, et al.
Journal Francais D'Ophtalmologie|October 6, 1998
[Update on a diagnostic test for choroideremia: the protein truncation test (PTT)]L Beaufrere, A Girardet, B Arnaud, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2016
[Genetics and molecular aspects of dystrophinopathies]F Leturcq, S Tuffery-Giraud
Ophthalmic Genetics|July 27, 1999
No missense mutation in choroideremia patients analyzed to dateL Beaufrère, M Claustres, S Tuffery
Human Mutation|January 1, 1992
A new intragenic polymorphism detected by the single-strand conformation polymorphism (SSCP) assay in the dystrophin geneS Tuffery, J Demaille, M Claustress
European Journal of Human Genetics : EJHG|January 1, 1996
Four novel dystrophin point mutations: detection by protein truncation test and transcript analysis in lymphocytes from Duchenne muscular dystrophy patientsS Tuffery, C Bareil, J Demaille, et al.
Human Genetics|May 1, 1995
Identification of variable length polyadenosine tract at the dystrophin locusS Tuffery, P Moine, J Demaille, et al.
Human Mutation|January 1, 1993
Base substitutions in the human dystrophin gene: detection by using the single-strand conformation polymorphism (SSCP) techniqueS Tuffery, P Moine, J Demaille, et al.
Annales De Biologie Clinique|August 5, 1999
[Genotypic diagnosis of Duchenne and Becker muscular dystrophies]S Tuffery-Giraud, S Chambert, J Demaille, et al.
Human Mutation|October 26, 1999
Point mutations in the dystrophin gene: evidence for frequent use of cryptic splice sites as a result of splicing defectsS Tuffery-Giraud, S Chambert, J Demaille, et al.
Journal Francais D'Ophtalmologie|October 6, 1998
[Retinoblastoma: importance of genetic counseling]A Girardet, L Beaufrere, S Tuffery, et al.
Journal Francais D'Ophtalmologie|October 6, 1998
[Update on a diagnostic test for choroideremia: the protein truncation test (PTT)]L Beaufrere, A Girardet, B Arnaud, et al.
Pageof 5