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F Munier

Showing results (41-50 of 54) with videos related to

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European Journal of Human Genetics : EJHG|April 10, 1999
Direct estimation of the recombination frequency between the RB1 gene and two closely linked microsatellites using sperm typingA Girardet, S Lien, E P Leeflang, et al.
Annales De Genetique|January 1, 1988
Cytogenetic analysis of 570 first trimester chorionic villi samplings: technique and resultsM Jotterand-Bellomo, G Pescia, H Nguyen The, et al.
Human Genetics|July 1, 1992
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility geneF Munier, M A Spence, G Pescia, et al.
Human Mutation|March 1, 2000
Identification of novel PAX6 mutations in two families with bilateral aniridia. Mutations in brief no. 167. OnlineM Neuner-Jehle, F Munier, A Kobetz, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 20, 2001
Leber's hereditary optic neuropathy mitochondrial DNA mutations in normal-tension glaucomaD Opial, M Boehnke, S Tadesse, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1992
[Loss of ganglion cells in the retina secondary to vincristine therapy]F Munier, S Uffer, C P Herbort, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1991
[Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients]F Munier, A Balmer, C von Moos, et al.
European Journal of Medical Genetics|December 5, 2022
Retinoblastoma: From genes to patient careY Bouchoucha, A Matet, A Berger, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
Ophthalmic Genetics|September 27, 2002
Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophyD Marchant, K Gogat, P Dureau, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
European Journal of Human Genetics : EJHG|April 10, 1999
Direct estimation of the recombination frequency between the RB1 gene and two closely linked microsatellites using sperm typingA Girardet, S Lien, E P Leeflang, et al.
Annales De Genetique|January 1, 1988
Cytogenetic analysis of 570 first trimester chorionic villi samplings: technique and resultsM Jotterand-Bellomo, G Pescia, H Nguyen The, et al.
Human Genetics|July 1, 1992
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility geneF Munier, M A Spence, G Pescia, et al.
Human Mutation|March 1, 2000
Identification of novel PAX6 mutations in two families with bilateral aniridia. Mutations in brief no. 167. OnlineM Neuner-Jehle, F Munier, A Kobetz, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 20, 2001
Leber's hereditary optic neuropathy mitochondrial DNA mutations in normal-tension glaucomaD Opial, M Boehnke, S Tadesse, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1992
[Loss of ganglion cells in the retina secondary to vincristine therapy]F Munier, S Uffer, C P Herbort, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1991
[Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients]F Munier, A Balmer, C von Moos, et al.
European Journal of Medical Genetics|December 5, 2022
Retinoblastoma: From genes to patient careY Bouchoucha, A Matet, A Berger, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
Ophthalmic Genetics|September 27, 2002
Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophyD Marchant, K Gogat, P Dureau, et al.
Pageof 6