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F L Munier

Showing results (31-40 of 59) with videos related to

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American Journal of Human Genetics|August 27, 1998
Gene localization for aculeiform cataract, on chromosome 2q33-35E Héon, S Liu, G Billingsley, et al.
Ophthalmic Genetics|January 23, 2002
MYOC mutation frequency in primary open-angle glaucoma patients from Western SwitzerlandA Mataftsi, F Achache, E Héon, et al.
Human Genetics|November 1, 1994
Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigreesF L Munier, L Arabien, P Flodman, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 27, 2016
Swiss Family with Dominant Stargardt Disease Caused by a Recurrent Mutation in the ELOVL4 GeneH V Tran, E Moret, V Vaclavik, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 24, 2005
[Optical coherence tomography in Malattia Leventinese]M-C Gaillard, T J Wolfensberger, S Uffer, et al.
American Journal of Human Genetics|December 5, 1998
Evidence of somatic and germinal mosaicism in pseudo-low-penetrant hereditary retinoblastoma, by constitutional and single-sperm mutation analysisF L Munier, F Thonney, A Girardet, et al.
Journal of Medical Genetics|November 25, 2003
A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataractC E Willoughby, Sara Arab, R Gandhi, et al.
Ophthalmic Genetics|November 12, 1998
Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosaE Millá, E Héon, P A Grounauer, et al.
Investigative Ophthalmology & Visual Science|January 14, 2000
Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2D Gill, R Klose, F L Munier, et al.
Investigative Ophthalmology & Visual Science|September 7, 1999
On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophiesE Korvatska, F L Munier, P Chaubert, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|August 27, 1998
Gene localization for aculeiform cataract, on chromosome 2q33-35E Héon, S Liu, G Billingsley, et al.
Ophthalmic Genetics|January 23, 2002
MYOC mutation frequency in primary open-angle glaucoma patients from Western SwitzerlandA Mataftsi, F Achache, E Héon, et al.
Human Genetics|November 1, 1994
Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigreesF L Munier, L Arabien, P Flodman, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 27, 2016
Swiss Family with Dominant Stargardt Disease Caused by a Recurrent Mutation in the ELOVL4 GeneH V Tran, E Moret, V Vaclavik, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 24, 2005
[Optical coherence tomography in Malattia Leventinese]M-C Gaillard, T J Wolfensberger, S Uffer, et al.
American Journal of Human Genetics|December 5, 1998
Evidence of somatic and germinal mosaicism in pseudo-low-penetrant hereditary retinoblastoma, by constitutional and single-sperm mutation analysisF L Munier, F Thonney, A Girardet, et al.
Journal of Medical Genetics|November 25, 2003
A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataractC E Willoughby, Sara Arab, R Gandhi, et al.
Ophthalmic Genetics|November 12, 1998
Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosaE Millá, E Héon, P A Grounauer, et al.
Investigative Ophthalmology & Visual Science|January 14, 2000
Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2D Gill, R Klose, F L Munier, et al.
Investigative Ophthalmology & Visual Science|September 7, 1999
On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophiesE Korvatska, F L Munier, P Chaubert, et al.
Pageof 6