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P Leroy

Showing results (351-360 of 438) with videos related to

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Investigative Ophthalmology & Visual Science|February 14, 2015
Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile NystagmusBasamat AlMoallem, Miriam Bauwens, Sophie Walraedt, et al.
Investigative Ophthalmology & Visual Science|December 15, 2015
Cobalamin C Deficiency Shows a Rapidly Progressing Maculopathy With Severe Photoreceptor and Ganglion Cell LossLucas Bonafede, Can H Ficicioglu, Leona Serrano, et al.
Scientific Reports|January 30, 2020
The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56Basamat Almoallem, Gavin Arno, Julie De Zaeytijd, et al.
Genes|September 28, 2021
The Phenotypic Spectrum of Patients with PHARC Syndrome Due to Variants in <i>ABHD12</i>: An Ophthalmic PerspectiveXuan-Thanh-An Nguyen, Hind Almushattat, Ine Strubbe, et al.
Molecular Genetics & Genomic Medicine|January 29, 2015
Novel insights into the molecular pathogenesis of CYP4V2-associated Bietti's retinal dystrophyGaluh D N Astuti, Vincent Sun, Miriam Bauwens, et al.
American Journal of Human Genetics|January 9, 2008
Biallelic mutation of BEST1 causes a distinct retinopathy in humansRosemary Burgess, Ian D Millar, Bart P Leroy, et al.
Investigative Ophthalmology & Visual Science|November 18, 2015
A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis PigmentosaKristof Van Schil, B Jeroen Klevering, Bart P Leroy, et al.
Acta Ophthalmologica|November 25, 2025
Vitreoretinal complications and surgical outcomes in patients with X-linked retinoschisisJonathan Hensman, Leo C Hahn, Mary J van Schooneveld, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|February 13, 2003
Genetic mapping of 66 new microsatellite (SSR) loci in bread wheatK. Gupta, S. Balyan, J. Edwards, et al.
Ophthalmic Genetics|December 5, 2022
Optic nerve involvement in <i>CACNA1F</i>-related disease: observations from a multicentric case seriesElisa Marziali, Filip Van Den Broeck, Sara Bargiacchi, et al.
Pageof 44

Showing results (351-360 of 438) with videos related to

Sort By:
Pageof 44
Investigative Ophthalmology & Visual Science|February 14, 2015
Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile NystagmusBasamat AlMoallem, Miriam Bauwens, Sophie Walraedt, et al.
Investigative Ophthalmology & Visual Science|December 15, 2015
Cobalamin C Deficiency Shows a Rapidly Progressing Maculopathy With Severe Photoreceptor and Ganglion Cell LossLucas Bonafede, Can H Ficicioglu, Leona Serrano, et al.
Scientific Reports|January 30, 2020
The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56Basamat Almoallem, Gavin Arno, Julie De Zaeytijd, et al.
Genes|September 28, 2021
The Phenotypic Spectrum of Patients with PHARC Syndrome Due to Variants in <i>ABHD12</i>: An Ophthalmic PerspectiveXuan-Thanh-An Nguyen, Hind Almushattat, Ine Strubbe, et al.
Molecular Genetics & Genomic Medicine|January 29, 2015
Novel insights into the molecular pathogenesis of CYP4V2-associated Bietti's retinal dystrophyGaluh D N Astuti, Vincent Sun, Miriam Bauwens, et al.
American Journal of Human Genetics|January 9, 2008
Biallelic mutation of BEST1 causes a distinct retinopathy in humansRosemary Burgess, Ian D Millar, Bart P Leroy, et al.
Investigative Ophthalmology & Visual Science|November 18, 2015
A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis PigmentosaKristof Van Schil, B Jeroen Klevering, Bart P Leroy, et al.
Acta Ophthalmologica|November 25, 2025
Vitreoretinal complications and surgical outcomes in patients with X-linked retinoschisisJonathan Hensman, Leo C Hahn, Mary J van Schooneveld, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|February 13, 2003
Genetic mapping of 66 new microsatellite (SSR) loci in bread wheatK. Gupta, S. Balyan, J. Edwards, et al.
Ophthalmic Genetics|December 5, 2022
Optic nerve involvement in <i>CACNA1F</i>-related disease: observations from a multicentric case seriesElisa Marziali, Filip Van Den Broeck, Sara Bargiacchi, et al.
Pageof 44