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Journal Francais D'Ophtalmologie
|
January 1, 1997
[Rapid genetic diagnosis of females carriers related to patients with choroideremia]
L Beaufrère, S Tuffery, C Hamel, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
An exonic polymorphism (381A/G) in the choroideremia gene
L Beaufrere, S Tuffery, C Hamel, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy
S Tuffery, P Moine, P Sarda, et al.
Experimental Eye Research
|
January 27, 1998
The protein truncation test (PTT) as a method of detection for choroideremia mutations
L Beaufrère, S Tuffery, C Hamel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 14, 2003
[Movement disorders in childhood: classification and genetic update]
A Roubertie, F Rivier, S Tuffery-Giraud, et al.
Human Genetics
|
December 1, 1991
Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies
M Claustres, S Tuffery, M P Chevron, et al.
Human Genetics
|
April 17, 1998
Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation test
S Tuffery, S Chambert, C Bareil, et al.
Revue Neurologique
|
May 2, 2002
[The varied etiologies of childhood-onset dystonia]
A Roubertie, F Rivier, V Humbertclaude, et al.
Investigative Ophthalmology & Visual Science
|
May 8, 2000
BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies
C F Schmitt-Bernard, C Guittard, B Arnaud, et al.
Journal of Neurosurgical Sciences
|
August 6, 2003
Treatment of dystonic syndromes by chronic electrical stimulation of the internal globus pallidus
L Cif, H El Fertit, N Vayssiere, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 43) with videos related to
Sort By:
Page
of 5
Journal Francais D'Ophtalmologie
|
January 1, 1997
[Rapid genetic diagnosis of females carriers related to patients with choroideremia]
L Beaufrère, S Tuffery, C Hamel, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
An exonic polymorphism (381A/G) in the choroideremia gene
L Beaufrere, S Tuffery, C Hamel, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1994
Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy
S Tuffery, P Moine, P Sarda, et al.
Experimental Eye Research
|
January 27, 1998
The protein truncation test (PTT) as a method of detection for choroideremia mutations
L Beaufrère, S Tuffery, C Hamel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 14, 2003
[Movement disorders in childhood: classification and genetic update]
A Roubertie, F Rivier, S Tuffery-Giraud, et al.
Human Genetics
|
December 1, 1991
Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies
M Claustres, S Tuffery, M P Chevron, et al.
Human Genetics
|
April 17, 1998
Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation test
S Tuffery, S Chambert, C Bareil, et al.
Revue Neurologique
|
May 2, 2002
[The varied etiologies of childhood-onset dystonia]
A Roubertie, F Rivier, V Humbertclaude, et al.
Investigative Ophthalmology & Visual Science
|
May 8, 2000
BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies
C F Schmitt-Bernard, C Guittard, B Arnaud, et al.
Journal of Neurosurgical Sciences
|
August 6, 2003
Treatment of dystonic syndromes by chronic electrical stimulation of the internal globus pallidus
L Cif, H El Fertit, N Vayssiere, et al.
Page
of 5