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F L Munier

Showing results (11-20 of 59) with videos related to

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Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 6, 2015
Potential blindness in children of patients with hereditary bone diseaseV Kheir, F L Munier, B Aubry-Rozier, et al.
Praxis|August 27, 1996
[Familial adenomatous polyposis]M T Constanda, F L Munier, S Caplin, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 24, 2005
Idiopathic cyclitic retrolental membrane in childrenC Oberhansli, F L Munier, S Uffer, et al.
Eye (London, England)|April 20, 2004
Clinical and immunopathological corneal phenotype in homozygotes for the BIGH3 R124H mutationC J M Diaper, D F Schorderet, P Chaubert, et al.
Praxis|August 27, 1996
[Retinoblastoma: clinical and molecular diagnostic aspects]F Thonney, F L Munier, A Balmer, et al.
Klinische Monatsblatter Fur Augenheilkunde|July 25, 1998
[Clinical study and genetic 3q28 locus linkage in 2 Swiss families with Kjer dominant optic atrophy (OPA1)]A Lefèvre, C Hiroz, L Zografos, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 29, 2014
Cone-rod dystrophy caused by a novel homozygous RPE65 mutation in Leber congenital amaurosisC Jakobsson, I S Othman, F L Munier, et al.
Ophthalmic Genetics|October 16, 1999
Rhegmatogenous retinal detachment after treatment of retinoblastomaE H Bovey, A Fernandez-Ragaz, E Héon, et al.
The British Journal of Ophthalmology|January 24, 2008
Genotype-phenotype correlation of age-related macular degeneration: influence of complement factor H polymorphismI Droz, I Mantel, A Ambresin, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1996
Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counselingF L Munier, F Thonney, A Balmer, et al.
Pageof 6

Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 6, 2015
Potential blindness in children of patients with hereditary bone diseaseV Kheir, F L Munier, B Aubry-Rozier, et al.
Praxis|August 27, 1996
[Familial adenomatous polyposis]M T Constanda, F L Munier, S Caplin, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 24, 2005
Idiopathic cyclitic retrolental membrane in childrenC Oberhansli, F L Munier, S Uffer, et al.
Eye (London, England)|April 20, 2004
Clinical and immunopathological corneal phenotype in homozygotes for the BIGH3 R124H mutationC J M Diaper, D F Schorderet, P Chaubert, et al.
Praxis|August 27, 1996
[Retinoblastoma: clinical and molecular diagnostic aspects]F Thonney, F L Munier, A Balmer, et al.
Klinische Monatsblatter Fur Augenheilkunde|July 25, 1998
[Clinical study and genetic 3q28 locus linkage in 2 Swiss families with Kjer dominant optic atrophy (OPA1)]A Lefèvre, C Hiroz, L Zografos, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 29, 2014
Cone-rod dystrophy caused by a novel homozygous RPE65 mutation in Leber congenital amaurosisC Jakobsson, I S Othman, F L Munier, et al.
Ophthalmic Genetics|October 16, 1999
Rhegmatogenous retinal detachment after treatment of retinoblastomaE H Bovey, A Fernandez-Ragaz, E Héon, et al.
The British Journal of Ophthalmology|January 24, 2008
Genotype-phenotype correlation of age-related macular degeneration: influence of complement factor H polymorphismI Droz, I Mantel, A Ambresin, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1996
Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counselingF L Munier, F Thonney, A Balmer, et al.
Pageof 6