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F L Munier

Showing results (41-50 of 59) with videos related to

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Gene Therapy|March 18, 2005
Lentiviral vector-mediated gene transfer in adult mouse photoreceptors is impaired by the presence of a physical barrierO Grüter, C Kostic, S V Crippa, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOXE Korvatska, F L Munier, L Zografos, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 27, 2007
Patient with Fanconi Syndrome (FS) and retinitis pigmentosa (RP) caused by a deletion and duplication of mitochondrial DNA (mtDNA)E M Pitchon, F Cachat, S Jacquemont, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigreesF L Munier, M X Wang, M A Spence, et al.
Biochemical and Biophysical Research Communications|July 29, 2000
Genomic characterization and embryonic expression of the mouse Bigh3 (Tgfbi) geneD F Schorderet, M Menasche, S Morand, et al.
Ophthalmic Genetics|March 1, 1997
Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastomaF L Munier, F Thonney, A Balmer, et al.
Ophthalmic Genetics|December 1, 1996
Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin geneB Piguet, E Héon, F L Munier, et al.
Gene Therapy|April 22, 2003
Activity analysis of housekeeping promoters using self-inactivating lentiviral vector delivery into the mouse retinaC Kostic, F Chiodini, P Salmon, et al.
American Journal of Human Genetics|February 17, 2001
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22E Héon, A D Paterson, M Fraser, et al.
Ophthalmic Genetics|March 23, 2001
Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patientsR I Bojinova, D F Schorderet, M C Addor, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
Gene Therapy|March 18, 2005
Lentiviral vector-mediated gene transfer in adult mouse photoreceptors is impaired by the presence of a physical barrierO Grüter, C Kostic, S V Crippa, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOXE Korvatska, F L Munier, L Zografos, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 27, 2007
Patient with Fanconi Syndrome (FS) and retinitis pigmentosa (RP) caused by a deletion and duplication of mitochondrial DNA (mtDNA)E M Pitchon, F Cachat, S Jacquemont, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigreesF L Munier, M X Wang, M A Spence, et al.
Biochemical and Biophysical Research Communications|July 29, 2000
Genomic characterization and embryonic expression of the mouse Bigh3 (Tgfbi) geneD F Schorderet, M Menasche, S Morand, et al.
Ophthalmic Genetics|March 1, 1997
Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastomaF L Munier, F Thonney, A Balmer, et al.
Ophthalmic Genetics|December 1, 1996
Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin geneB Piguet, E Héon, F L Munier, et al.
Gene Therapy|April 22, 2003
Activity analysis of housekeeping promoters using self-inactivating lentiviral vector delivery into the mouse retinaC Kostic, F Chiodini, P Salmon, et al.
American Journal of Human Genetics|February 17, 2001
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22E Héon, A D Paterson, M Fraser, et al.
Ophthalmic Genetics|March 23, 2001
Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patientsR I Bojinova, D F Schorderet, M C Addor, et al.
Pageof 6