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F Munier

Showing results (31-40 of 54) with videos related to

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Journal Francais D'Ophtalmologie|January 1, 1995
[Regressive bilateral retinoblastoma. Clinical and genetic study. Apropos of a case]S Marrakchi, H Bouguila, M Ghorbal, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1989
Constitutional karyotype in retinoblastoma. Case report and review of literatureF Munier, G Pescia, M Jotterand-Bellomo, et al.
Journal Francais D'Ophtalmologie|February 13, 2016
[Genotype-phenotype correlation in ten Tunisian families with non-syndromic retinitis pigmentosa]A Chebil, Y Falfoul, I Habibi, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 27, 2016
Multimodal Imaging of Retinal Astrocytic Hamartoma Associated with Congenital Hypertrophy of Retinal Pigment EpitheliumC Trojman, L Zografos, A Dirani, et al.
The British Journal of Ophthalmology|March 19, 2003
Pulverulent cataract with variably associated microcornea and iris coloboma in a MAF mutation familyR V Jamieson, F Munier, A Balmer, et al.
Human Genetics|March 1, 1988
A "new" allele of esterase D in a retinoblastoma familyF Munier, G Pescia, A Balmer, et al.
American Journal of Human Genetics|January 13, 2000
Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typingA Girardet, M S McPeek, E P Leeflang, et al.
The British Journal of Dermatology|June 24, 2006
Pseudoxanthoma elasticum: evaluation of diagnostic criteria based on molecular dataS Christen-Zäch, M Huber, B Struk, et al.
Klinische Monatsblatter Fur Augenheilkunde|July 25, 1998
[Mutational screening of peripherin/RDS genes, rhodopsin and ROM-1 in 69 index cases with retinitis pigmentosa and other retinal dystrophies]E Millá, E Héon, B Piguet, et al.
International Ophthalmology Clinics|January 1, 1993
Molecular genetics of retinoblastomaK Zhang, M X Wang, F Munier, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Journal Francais D'Ophtalmologie|January 1, 1995
[Regressive bilateral retinoblastoma. Clinical and genetic study. Apropos of a case]S Marrakchi, H Bouguila, M Ghorbal, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1989
Constitutional karyotype in retinoblastoma. Case report and review of literatureF Munier, G Pescia, M Jotterand-Bellomo, et al.
Journal Francais D'Ophtalmologie|February 13, 2016
[Genotype-phenotype correlation in ten Tunisian families with non-syndromic retinitis pigmentosa]A Chebil, Y Falfoul, I Habibi, et al.
Klinische Monatsblatter Fur Augenheilkunde|April 27, 2016
Multimodal Imaging of Retinal Astrocytic Hamartoma Associated with Congenital Hypertrophy of Retinal Pigment EpitheliumC Trojman, L Zografos, A Dirani, et al.
The British Journal of Ophthalmology|March 19, 2003
Pulverulent cataract with variably associated microcornea and iris coloboma in a MAF mutation familyR V Jamieson, F Munier, A Balmer, et al.
Human Genetics|March 1, 1988
A "new" allele of esterase D in a retinoblastoma familyF Munier, G Pescia, A Balmer, et al.
American Journal of Human Genetics|January 13, 2000
Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typingA Girardet, M S McPeek, E P Leeflang, et al.
The British Journal of Dermatology|June 24, 2006
Pseudoxanthoma elasticum: evaluation of diagnostic criteria based on molecular dataS Christen-Zäch, M Huber, B Struk, et al.
Klinische Monatsblatter Fur Augenheilkunde|July 25, 1998
[Mutational screening of peripherin/RDS genes, rhodopsin and ROM-1 in 69 index cases with retinitis pigmentosa and other retinal dystrophies]E Millá, E Héon, B Piguet, et al.
International Ophthalmology Clinics|January 1, 1993
Molecular genetics of retinoblastomaK Zhang, M X Wang, F Munier, et al.
Pageof 6