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J M Rozet

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

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Human Genetics|July 31, 2019
Genetic architecture of retinoic-acid signaling-associated ocular developmental defectsB Nedelec, J-M Rozet, L Fares Taie
Pediatrie|January 1, 1992
[Molecular genetics and prenatal diagnosis]S Lyonnet, J M Rozet, C Martin, et al.
Journal Francais D'Ophtalmologie|January 1, 1996
[Rapid demonstration of mutations previously identified in parents at risk of patients with autosomic dominant retinitis pigmentosa]E Souied, J M Rozet, S Gerber, et al.
Journal Francais D'Ophtalmologie|March 16, 2005
[Hereditary macular dystrophies]J-M Rozet, S Gerber, D Ducroq, et al.
Genomics|July 15, 1994
Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1L Oliveira, P Miniou, E Viegas-Pequignot, et al.
Human Genetics|April 1, 1995
Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's diseaseS Gerber, J M Rozet, D Bonneau, 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 of Medical Genetics|May 1, 1993
X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locusD Bonneau, J M Rozet, C Bulteau, 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.
Pageof 5

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

Sort By:
Pageof 5
Human Genetics|July 31, 2019
Genetic architecture of retinoic-acid signaling-associated ocular developmental defectsB Nedelec, J-M Rozet, L Fares Taie
Pediatrie|January 1, 1992
[Molecular genetics and prenatal diagnosis]S Lyonnet, J M Rozet, C Martin, et al.
Journal Francais D'Ophtalmologie|January 1, 1996
[Rapid demonstration of mutations previously identified in parents at risk of patients with autosomic dominant retinitis pigmentosa]E Souied, J M Rozet, S Gerber, et al.
Journal Francais D'Ophtalmologie|March 16, 2005
[Hereditary macular dystrophies]J-M Rozet, S Gerber, D Ducroq, et al.
Genomics|July 15, 1994
Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1L Oliveira, P Miniou, E Viegas-Pequignot, et al.
Human Genetics|April 1, 1995
Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's diseaseS Gerber, J M Rozet, D Bonneau, 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 of Medical Genetics|May 1, 1993
X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locusD Bonneau, J M Rozet, C Bulteau, 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.
Pageof 5