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I Perrault

Showing results (1-10 of 30) with videos related to

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Anesthesia Progress|January 1, 1990
Effects of articaine on intrapulpal, mandibular, and femoral pressures in dogsS Simard-Savoie, I Perrault, M J Perron
Advances in Experimental Medicine and Biology|January 8, 2021
Heimler SyndromeS Mechaussier, I Perrault, H Dollfus, et al.
Human Genetics|June 1, 1996
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13A Camuzat, J M Rozet, H Dollfus, et al.
Journal Francais D'Ophtalmologie|March 16, 2005
[Leber congenital amaurosis: comprehensive survey of genetic heterogeneity. A clinical definition update]S Hanein, I Perrault, S Gerber, et al.
Journal Francais D'Ophtalmologie|January 9, 2010
[First North African observation of Leber congenital amaurosis secondary to CEP290 gene mutation]N Aboussair, A Berahou, I Perrault, et al.
Journal of Medical Genetics|July 5, 2003
Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null alleleI Perrault, S Hanein, S Gerber, et al.
American Journal of Human Genetics|March 26, 1999
A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3A Cabot, J M Rozet, S Gerber, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
Complete abolition of the retinal-specific guanylyl cyclase (retGC-1) catalytic ability consistently leads to leber congenital amaurosis (LCA)J M Rozet, I Perrault, S Gerber, et al.
Journal of Medical Genetics|April 16, 2002
Dominant X linked retinitis pigmentosa is frequently accounted for by truncating mutations in exon ORF15 of the RPGR geneJ-M Rozet, I Perrault, N Gigarel, et al.
Investigative Ophthalmology & Visual Science|January 14, 2000
ABCR gene analysis in familial exudative age-related macular degenerationE H Souied, D Ducroq, J M Rozet, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Anesthesia Progress|January 1, 1990
Effects of articaine on intrapulpal, mandibular, and femoral pressures in dogsS Simard-Savoie, I Perrault, M J Perron
Advances in Experimental Medicine and Biology|January 8, 2021
Heimler SyndromeS Mechaussier, I Perrault, H Dollfus, et al.
Human Genetics|June 1, 1996
Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13A Camuzat, J M Rozet, H Dollfus, et al.
Journal Francais D'Ophtalmologie|March 16, 2005
[Leber congenital amaurosis: comprehensive survey of genetic heterogeneity. A clinical definition update]S Hanein, I Perrault, S Gerber, et al.
Journal Francais D'Ophtalmologie|January 9, 2010
[First North African observation of Leber congenital amaurosis secondary to CEP290 gene mutation]N Aboussair, A Berahou, I Perrault, et al.
Journal of Medical Genetics|July 5, 2003
Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null alleleI Perrault, S Hanein, S Gerber, et al.
American Journal of Human Genetics|March 26, 1999
A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3A Cabot, J M Rozet, S Gerber, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
Complete abolition of the retinal-specific guanylyl cyclase (retGC-1) catalytic ability consistently leads to leber congenital amaurosis (LCA)J M Rozet, I Perrault, S Gerber, et al.
Journal of Medical Genetics|April 16, 2002
Dominant X linked retinitis pigmentosa is frequently accounted for by truncating mutations in exon ORF15 of the RPGR geneJ-M Rozet, I Perrault, N Gigarel, et al.
Investigative Ophthalmology & Visual Science|January 14, 2000
ABCR gene analysis in familial exudative age-related macular degenerationE H Souied, D Ducroq, J M Rozet, et al.
Pageof 3